Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2396-79-4

Post Buying Request

2396-79-4 Suppliers

Recommended suppliersmore

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

2396-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2396-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2396-79:
(6*2)+(5*3)+(4*9)+(3*6)+(2*7)+(1*9)=104
104 % 10 = 4
So 2396-79-4 is a valid CAS Registry Number.

2396-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name E,Z-4-hexenecarboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl (E,Z)-hex-4-enoate

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:2396-79-4 SDS

2396-79-4Relevant articles and documents

Preparation, crystal structure and reactivity of bis(methylacrylate)(pyridine)nickel(0)

Sustmann, Reiner,Hopp, Peter,Boese, Roland

, p. 259 - 264 (1989)

The preparation, crystal structure and reactivity of bis(methyl acrylate)(pyridine)nickel(0) are reported.This complex reacts with E,Z-1-bromo-1-propene in the presence of water to give the conjugate addition product.Complexes of this type seem to be invo

Linear Selective Isomerization/Hydroformylation of Unsaturated Fatty Acid Methyl Esters: A Bimetallic Approach

Gaide, Tom,Bianga, Jonas,Schlipk?ter, Kim,Behr, Arno,Vorholt, Andreas J.

, p. 4163 - 4171 (2017/06/19)

Herein, we report about the development of an isomerization/hydroformylation tandem reaction to selectively convert fatty acid methyl esters into asymmetric α,ω-functionalized aldehyde esters. An orthogonal tandem catalytic system consisting of a palladium-based isomerization catalyst and a rhodium-based hydroformylation catalyst was developed, using methyl 3-hexenoate as a model substrate. Using this catalyst, high yields (81% at 99% conversion) and regioselectivities (l/b-ratio of 98/2) toward the desired terminal hydroformylation product are obtained in the conversion of methyl 3-hexenoate under mild conditions. Ethyl 4-decenoate was subsequently applied as a second model substrate to identify challenges associated with the longer chain length of the unsaturated ester. Finally, methyl oleate was converted using the developed catalyst system. High aldehyde yields of 74% (at 99% conversion) with an l/b-ratio of 91/9 are obtained.

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 2396-79-4