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CH2=C-CH2C1
— REACTS READIIY THROUGH BOTH ITS C l ATOM AND DOUBU BOND Wé-.
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AVAILABLE m COMMIitClÂl QUANTITIES The reactions of this important compound are characterized by rapidity and freedom from by-products· Reylacement of the chlorine atom leads t o a variety of compounds having widely different structures. The double bond can be reacted with a variety of reagents to give products useful for the further synthesis of a large number of chemicals, pharmaceuticals and anaesthetics.
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The following are examples of replacement and double bond reactions : Br2CH 2 Br-CHBi-CH 2 Cl {1-chloro-2,3-dibromopropane) CH2 = CH-CH 2 C1 + CuCN * CH 2 =CH-CH 2 CN + CuCl (allyl cyanide) CH 2 =CH-CH 2 C1 + NaOR CH,=CH-CH 2 OR + NaCI (alkyl allyl ether)
CH 2 = CH-CH 2 C1
44.9°c AareofropfcOcta Refi ractive index, N „ 20
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Other Shell Chemical products include : Allyl Alcohol, Cyclohexane, Diisobutylene, Acetone and Methyl Ethyl Ketone.
For data sheets and a sample, if desired, write
to
SHELL CHEMICAL CORPORATION 100 Bush Street, San Francisco 6 · 500 Fifth Avenue, New York 18 Los Angeles · Houston · St. Louis · Chicago · Cleveland · Boston · Detroit
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