Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13361-32-5

Post Buying Request

13361-32-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13361-32-5 Usage

Description

Allyl cyanoacetate, also known as 3-(2-propenyl)-2-cyanoacetic acid, is an organic compound that serves as an intermediate for the production of various chemicals and materials. It is a liquid with unique chemical properties, making it a versatile component in the synthesis of different products.

Uses

Used in Chemical Synthesis:
Allyl cyanoacetate is used as an intermediate for the production of special adhesives. Its unique chemical structure allows it to be a key component in the formulation of these adhesives, enhancing their bonding properties and performance.
Used in Pharmaceutical Industry:
Allyl cyanoacetate is also utilized in the pharmaceutical industry for the synthesis of various drugs and pharmaceutical compounds. Its reactivity and compatibility with other molecules make it a valuable building block in the development of new medications.
Used in Polymer Industry:
In the polymer industry, allyl cyanoacetate is used as a monomer in the production of polymers with specific properties. Its incorporation into polymer chains can lead to materials with enhanced characteristics, such as improved strength, flexibility, or chemical resistance.
Used in Dye and Pigment Industry:
Allyl cyanoacetate is employed in the synthesis of dyes and pigments, where its chemical properties contribute to the development of vibrant and stable colorants for various applications, including textiles, plastics, and printing inks.
Used in Agricultural Industry:
In the agricultural sector, allyl cyanoacetate is used as a building block for the development of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of effective and targeted products for crop protection and management.
Overall, allyl cyanoacetate is a versatile compound with a wide range of applications across different industries, thanks to its unique chemical properties and reactivity.

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

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • 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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 13361-32-5