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13361-32-5

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13361-32-5 Usage

Chemical Properties

Liquid

Uses

Allyl cyanoacetate is an intermediate for special adhesives. Product Data Sheet

Check Digit Verification of cas no

The CAS Registry Mumber 13361-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13361-32:
(7*1)+(6*3)+(5*3)+(4*6)+(3*1)+(2*3)+(1*2)=75
75 % 10 = 5
So 13361-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2/c1-2-5-9-6(8)3-4-7/h2H,1,3,5H2

13361-32-5 Well-known Company Product Price

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  • Aldrich

  • (360961)  Allylcyanoacetate  98%

  • 13361-32-5

  • 360961-25G

  • 926.64CNY

  • Detail

13361-32-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Allyl Cyanoacetate

1.2 Other means of identification

Product number -
Other names Allyl cyanoacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13361-32-5 SDS

13361-32-5Relevant articles and documents

IMINIUM SALTS AND METHODS OF PREPARING ELECTRON DEFICIENT OLEFINS USING SUCH NOVEL IMINIUM SALTS

-

Page/Page column 32-33, (2008/12/05)

This invention relates to novel iminium salts, which may be in the form of ionic liquids, and a process for producing electron deficient olefins, such as 2-cyanoacrylates, using such an iminium salt, for instance in the form of an ionic liquid.

ESTERIFICATION OF CARBOXYLIC ACIDS WITH ALLYL ALCOHOL

D'yachkov, A. I.,Likhterov, V. R.,Etlis, V. S.

, p. 829 - 832 (2007/10/02)

The kinetics of the esterification of substituted carboxylic acids with allyl alcohol were studied.The reaction is of first order in the catalyst and in the substrate, and the equilibrium under the investigated conditions is shifted toward the formation of the ester.The observed enthalpy of activation does not depend on the substituent, and the difference in the reactivities of the investigated compounds is determined entirely by the entropy component of the free energy.

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