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7596-39-6

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7596-39-6 Usage

General Description

(Z)-2-propan-2-ylbut-2-enedioic acid, also known as diethylsuccinic acid, is a chemical compound with the molecular formula C8H14O4. It is a colorless, crystalline solid and is often used as an intermediate in the synthesis of various pharmaceuticals and fine chemicals. (Z)-2-propan-2-ylbut-2-enedioic acid is a dicarboxylic acid, meaning it contains two carboxylic acid functional groups. It is known for its wide range of applications, including its use as a corrosion inhibitor, a food additive, and as a building block for the synthesis of various organic compounds. Its structure and properties make it a versatile and important chemical in the field of organic synthesis and in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7596-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7596-39:
(6*7)+(5*5)+(4*9)+(3*6)+(2*3)+(1*9)=136
136 % 10 = 6
So 7596-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O4/c1-4(2)5(7(10)11)3-6(8)9/h3-4H,1-2H3,(H,8,9)(H,10,11)/b5-3-

7596-39-6SDS

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 (Z)-2-propan-2-ylbut-2-enedioic acid

1.2 Other means of identification

Product number -
Other names Isopropyl-fumarsaeure

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:7596-39-6 SDS

7596-39-6Relevant articles and documents

Asymmetric synthesis of 2-substituted butane-1,4-diols by hydrogenation of homochiral fumaramide derivatives

Jawaid, Samaila,Farrugia, Louis J.,Robins, David J.

, p. 3979 - 3988 (2007/10/03)

Diastereoselective hydrogenation of homochiral fumaramides 1 derived from (2R)-Oppolzer's sultam was observed by analysis of the 1H NMR spectra of the succinamide mixtures with de's of 77-88%. Reduction of these succinamides using LiAlH4 gave the corresponding (2S)-butane-1,4- diols and established that addition of hydrogen takes place selectively on the re-face of fumaramides 1. The stereoselectivity was confirmed by estimating the ee's from the 19F NMR spectra of the Mosher's diesters of the diols. This methodology was applied to the synthesis of selected pyrrolidine natural products in homochiral form.

Enantiospecific synthesis of 3-substituted aspartic acids via enzymic amination of substituted fumaric acids

Akhtar,Botting,Cohen,Gani

, p. 5899 - 5908 (2007/10/02)

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