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        <title>Organic Chemistry Message Board</title>
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        <![CDATA[ An organic chemistry question-answer forum ]]>
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		<item>
			<title><![CDATA[ Cyromazine-insecticide and an acaricide ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1687/t/Cyromazine-insecticide-and-an-acaricide.html</link>
			<description><![CDATA[ <a target="_blank" href="http://www.lookchem.com/Cyromazine/">Cyromazine</a> is is a cyclopropyl derivative of melamine.It is a triazine insect growth regulator used as an
insecticide and an acaricide.
<br>
Cyromazine works by affecting the nervous system of the immature larval stages of certain insects.In veterinary medicine, cyromazine is used as a
ectoparasiticide. ]]></description>

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			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1687</guid>
			<pubDate>Fri, 06 Nov 2009 07:52:21 GMT</pubDate>
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		<item>
			<title><![CDATA[ a Antihypertensive Drug-Cilnidipine ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1686/t/a-Antihypertensive-Drug-Cilnidipine.html</link>
			<description><![CDATA[ <p><a target="_blank" href="http://www.lookchem.com/Cilnidipine/">Cilnidipine</a> is a dual blocker of L-type voltage-gated Ca2+ channels in vascular smooth muscle and N-type
Ca2+ channels in sympathetic nerve terminals that supply blood vessels.
<br>
Cilnidipine has been developed as a slow-onset and long-lasting antihypertensive drug in Japan.
<br>
Recent electrophysiological data indicate that cilnidipine might be a dual-channel antagonist for peripheral neuronal N-type and vascular L-type... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1686</guid>
			<pubDate>Fri, 06 Nov 2009 07:51:06 GMT</pubDate>
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			<title><![CDATA[ Dimethoate ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1685/t/Dimethoate.html</link>
			<description><![CDATA[ <p><a target="_blank" href="http://www.lookchem.com/Dimethoate/">Dimethoate</a> is a widely used organophosphate insecticide used to kill insects on contact. It was patented
and introduced in the 1950s by American Cyanamid. Like other organophosphates, dimethoate is an anticholinesterase which disables cholinesterase, an enzyme
essential for central nervous system function.
<br></p> ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1685</guid>
			<pubDate>Fri, 06 Nov 2009 07:49:37 GMT</pubDate>
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		</item>
		<item>
			<title><![CDATA[ Sodium bicarbonate ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1684/t/Sodium-bicarbonate.html</link>
			<description><![CDATA[ <p><a target="_blank" href="http://www.lookchem.com/SODIUM-BICARBONATE/">Sodium bicarbonate</a>(144-55-<img src="http://www.ezboard.com/images/emoticons/glasses.gif"> is a white crystalline solid material and odorless. It  is widely
used in the food industry, in making rubber; in pharmaceuticals; as an antacid; in fire extinguishers, soap and detergents, rug cleaners, animal feeds, and
textiles; in leather preparation; in soap, detergent, and paper manufacturing; for flue-gas scrubbing; and... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1684</guid>
			<pubDate>Fri, 06 Nov 2009 07:24:59 GMT</pubDate>
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		</item>
		<item>
			<title><![CDATA[ What effect might sulfuric acid have on the environment? ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1683/t/What-effect-might-sulfuric-acid-have-on-the-environment-.html</link>
			<description><![CDATA[ <p><a target="_blank" href="http://www.lookchem.com/2-Ethoxyethanol/">Sulfuric</a> acid will exist as particles or droplets in the air if released to the
atmosphere. It dissolves when mixed with water. It</p>

<p>has moderate acute (short-term) toxicity on aquatic life. Sulfuric acid is very corrosive and would badly burn any plants, birds or</p>

<p>land animals exposed to it. It has moderate chronic (long-term) toxicity to aquatic life. Chronic effects on plants, birds or land</p>... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1683</guid>
			<pubDate>Fri, 06 Nov 2009 07:23:50 GMT</pubDate>
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			<title><![CDATA[ sodium chlorate ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1682/t/sodium-chlorate.html</link>
			<description><![CDATA[ <p>When pure, <a target="_blank" href="http://www.lookchem.com/SODIUM-CHLORATE/">sodium chlorate</a>(7775-09-9) is a white crystalline powder that is readily soluble in water.
It is hygroscopic. It decomposes above 250 °C to release oxygen and leave sodium chloride.
<br>
Sodium chlorate is used as a non-selective herbicide. It is considered phytotoxic to all green plant parts. It can also kill through root absorption.
<br>
Sodium chlorate is manufactured by the electrolysis of saturated,... ]]></description>

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			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1682</guid>
			<pubDate>Fri, 06 Nov 2009 07:20:38 GMT</pubDate>
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			<title><![CDATA[ What effect might 2-Ethoxyethanol have on my health? ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1681/t/What-effect-might-2-Ethoxyethanol-have-on-my-health-.html</link>
			<description><![CDATA[ <a target="_blank" href="http://www.lookchem.com/2-Ethoxyethanol/">2-Ethoxyethanol</a> can effect you when breathed in or by passing through your skin.
Short-term exposures may irritate the eyes, nose, and throat. Very high levels may cause you to feel dizzy, lightheaded and to pass out. Long-term effects from
exposure to 2-Ethoxyethanol are possible kidney damage, damaged blood cells, damaged testes in males, and decreased fertility in males. 2-Ethoxyethanol has
been shown to be a teratogen... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1681</guid>
			<pubDate>Fri, 06 Nov 2009 07:11:04 GMT</pubDate>
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		<item>
			<title><![CDATA[ about Conjugated linoleic acid ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1680/t/about-Conjugated-linoleic-acid.html</link>
			<description><![CDATA[ <a target="_blank" href="http://www.imaginechem.com/product/prodetail-13727.html">Conjugated linoleic acids</a> (CLA) are a family of at least 28 isomers of linoleic acid
found especially in the meat and dairy products derived from ruminants. As the name implies, the double bonds of CLAs are conjugated.
<br>
CLAs were discovered accidentally by researchers looking for mutagens in beef. The dairy and beef industries have taken note of CLA&#39;s healthy benefits and
are researching the natural... ]]></description>

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			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1680</guid>
			<pubDate>Wed, 04 Nov 2009 21:21:33 GMT</pubDate>
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			<title><![CDATA[ 1H NMR & IR : unknown structure determination ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1679/t/1H-NMR-IR-unknown-structure-determination.html</link>
			<description><![CDATA[ Hi all,
<br>
<br>
I was struggling in solving this question which is a part of a practice exam, and I need you to be patient with me and teach me step by step how to figure out
the structure and how to read and analyze the spectra.
<br>
<br>
I attached the two 1H NMR &amp; IR spectra so you will be able to know what structure I&#39;m talking about.
<br>
<br>
I started with finding the saturation number which is 5 so I know that at least I have aromatic ring and double bond(s)
<br>
I predicted... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (dead actor)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1679</guid>
			<pubDate>Sun, 01 Nov 2009 17:59:51 GMT</pubDate>
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			<title><![CDATA[ 1-acetyl-2-phenyl hydrazine ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1678/t/1-acetyl-2-phenyl-hydrazine.html</link>
			<description><![CDATA[ <font face="Verdana">1-acetyl-2-phenyl hydrazine
<br>
<a target="_blank" href="http://www.nbfinchem.com.cn/product/prodetail-1240.html">1-acetyl-2-phenyl hydrazine</a> is white to light yellow crystal powder with its formula
C8H10N2O. It is chemical raw material and slightly soluble in water.
<br>
Its synonyms are... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1678</guid>
			<pubDate>Sat, 31 Oct 2009 21:45:30 GMT</pubDate>
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		<item>
			<title><![CDATA[ 3,4-diaminobenzoic acid ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1677/t/3-4-diaminobenzoic-acid.html</link>
			<description><![CDATA[ 3,4-diaminobenzoic acid
<br>
<a target="_blank" href="http://www.nbfinchem.com.cn/product/prodetail-1243.html">3,4-diaminobenzoic acid</a> is chemical raw material, and often used as intermediate. I have
read about some process about it. Take follows for example.
<br>
3,4-diaminobenzoic acid is an intermediate for the preparation of poly[2,5(6)-benzimidazole], a polymer having excellent high temperature properties and
resistance to acid hydrolysis. Known methods of preparing... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1677</guid>
			<pubDate>Sat, 31 Oct 2009 21:29:20 GMT</pubDate>
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		<item>
			<title><![CDATA[ 2,4-DIAMINO MESITYLENE ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1676/t/2-4-DIAMINO-MESITYLENE.html</link>
			<description><![CDATA[ <a target="_blank" href="http://www.nbfinchem.com.cn/product/prodetail-1246.html">2,4-DIAMINO MESITYLENE</a> is a light yellow to brown crystal powder, it is used as
intermediate for dyestuff and pharmaceuticals.
<br>
It has some synonyms such as
2,4,6-trimethyl-1,3-benzenediamine;2,4,6-trimethyl-3-benzenediamine;1,3-DIAMINO-2,4,6-TRIMETHYLBENZENE;2,4-DIAMINOMESITYLENE;2,4-DIAMINO-1,3,5-TRIMETHYLBENZENE. ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1676</guid>
			<pubDate>Sat, 31 Oct 2009 20:52:39 GMT</pubDate>
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			<title><![CDATA[ Benzene ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1675/t/Benzene.html</link>
			<description><![CDATA[ Ok so I have a question about naming benzene rings            . <img style="width: 89px; height: 152px;" alt="http://www.chemvc.com/~tim/1,4-dimethylbenzene.jpg" src="http://www.chemvc.com/%7Etim/1,4-dimethylbenzene.jpg"> Does 1,4 dimethylbenzene have to be orginized
like this or can it be written on top right and bottom left
<br> ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (Jason123)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1675</guid>
			<pubDate>Sat, 31 Oct 2009 19:36:47 GMT</pubDate>
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			<title><![CDATA[ Tetraphenyltin ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1674/t/Tetraphenyltin.html</link>
			<description><![CDATA[ <p><a target="_blank" href="http://www.nbfinchem.com.cn/product/prodetail-1235.html">Tetraphenyltin</a> is an off-white crystal powder, and often used as chemical catalyst.
<br>
It is insoluble in water and has melting point  223-229 °C, Boiling point  420 °C, Flash point  111 °C.
<br>
It has some synonyms, such as Tetraphenyltin, Tetraphenylstannane, Stannane, tetraphenyl-, Tin tetraphenyl, TETRAPHENYL TIN.</p> ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1674</guid>
			<pubDate>Sat, 31 Oct 2009 07:55:42 GMT</pubDate>
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			<title><![CDATA[ Effects of Benidipine on Daytime Blood Pressure Changes in Patients with Essential Hypertension ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1673/t/Effects--Benidipine--Daytime-Blood-Pressure-Changes--Patient.html</link>
			<description><![CDATA[ The effects of long-term acting dihydropyridine calcium antagonists on daytime blood pressure (BP) changes and autonomic nervous activity have not been fully
evaluated in patients with essential hypertension (EH). We assessed the changes in 24-h BP and position-related BP during daytime induced by benidipine in EH
patients by using ambulatory BP monitoring (ABPM) devices equipped with a body-position sensor. Research design and methods: Nineteen patients with EH had ABPM
before and after... ]]></description>

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			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1673</guid>
			<pubDate>Sat, 31 Oct 2009 06:49:36 GMT</pubDate>
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			<title><![CDATA[ asymmetric hydrogenation of olefin prochiral substrate ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1672/t/asymmetric-hydrogenation-of-olefin-prochiral-substrate.html</link>
			<description><![CDATA[ <p>Dear all,</p>

<p>Now I am doing a research about producing chiral compound from olefin base prochiral substrate. I have tried to utilize short chain of olefin substrate such
as dimethyl itaconate until dibutyl itaconate, but the results were not satisfying enough. Actually I want to try other olefin substrate with more bulky group
which usually contain phenyl group. But I face a problem that usually the more bulky olefinic compounds exist in carboxylic acid form. Then I have to convert
to... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (kiky)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1672</guid>
			<pubDate>Thu, 29 Oct 2009 00:30:12 GMT</pubDate>
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		</item>
		<item>
			<title><![CDATA[ Cancer Chemotherapy Diet ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1671/t/Cancer-Chemotherapy-Diet.html</link>
			<description><![CDATA[ <font face="Verdana"><img height="15" src="http://www.ezboard.com/images/emoticons/smile.gif" width="15" alt="image">A nutritious diet during chemotherapy
tends to decrease the severeness of the side effects of chemotherapy. It also increases the effectiveness of chemotherapy, and thus decreases its duration,
because a well nourished body responds well to cancer treatment.
<br>
Cancer chemotherapy diet should include foods high in proteins, such as eggs, nuts, dairy and beans. Vegetables,... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1671</guid>
			<pubDate>Wed, 28 Oct 2009 02:44:44 GMT</pubDate>
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			<title><![CDATA[ 2,4-Dichlorophenoxyacetic acid ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1670/t/2-4-Dichlorophenoxyacetic-acid.html</link>
			<description><![CDATA[ 2,4-Dichlorophenoxyacetic acid  is a common systemic herbicide used in the control of broadleaf weeds. It is the most widely used herbicide in the world,
and the third most commonly used in North America.2,4-Dichlorophenoxyacetic acid is also an important synthetic auxin, often used in laboratories for plant
research and as a supplement in plant cell culture media such as MS medium.But do you know the history of it?
<br>
   2,4-Dichlorophenoxyacetic acid was developed during World War II by a... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (vivianbao)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1670</guid>
			<pubDate>Sun, 25 Oct 2009 07:09:30 GMT</pubDate>
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		<item>
			<title><![CDATA[ CLINICAL PHARMACOLOGY of Pemirolast potassium ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1669/t/CLINICAL-PHARMACOLOGY-of-Pemirolast-potassium.html</link>
			<description><![CDATA[ <p><font face="Verdana">   Pemirolast potassium is a slightly yellow, water-soluble powder with a molecular formula of C10H7KN6O, molecular weight of 266.3,its
Chemical name is 9-methyl-3-(1H-tetrazol-5-yl)-4H-pyrido[1,2-α] pyrimidin-4-one potassium.Pemirolast potassium is used for long-term treatment of bronchial
asthma.
<br>
   <a target="_blank" href="http://www.borunchem.com.cn/product/prodetail-1685.html">Pemirolast potassium</a> had no effect on mating and fertility in rats at oral... ]]></description>

			<!-- optional elements -->
			<author>feeds@yuku.com (vivianbao)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1669</guid>
			<pubDate>Sun, 25 Oct 2009 07:08:00 GMT</pubDate>
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			<title><![CDATA[ NYC Sting Uncovers ＇Gun Show Loophole＇ ]]></title>
			<link>http://organicchemistrymessageboard.yuku.com/topic/1668/t/NYC-Sting-Uncovers-Gun-Show-Loophole-.html</link>
			<description><![CDATA[ <p><font face="Verdana">Investigators hired by New York City conducted stings at gun shows in states that have not closed the &quot;gun show loophole&quot; and
found some vendors openly selling weapons to buyers who admitted they couldn&#39;t pass background checks.</font></p>

<p><font face="Verdana">The stings, described in a city report released Wednesday, were conducted at seven gun shows in Tennessee, Ohio and Nevada. Those
states are among the many that permit private unlicensed... ]]></description>

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			<author>feeds@yuku.com (sunnye)</author>
			<guid isPermaLink="true">http://organicchemistrymessageboard.yuku.com/topic/1668</guid>
			<pubDate>Fri, 23 Oct 2009 16:02:29 GMT</pubDate>
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