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630-51-3

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630-51-3 Usage

General Description

2,2,3,3-Tetramethylsuccinic acid, 97 is a chemical compound with a purity of 97%. It is a white crystalline powder that is used in various industrial applications, including as a building block for the synthesis of other organic compounds. This chemical is commonly used in the production of pharmaceuticals, agricultural chemicals, and polymers. It is also used as a reagent in research laboratories for organic synthesis and as a chemical intermediate. 2,2,3,3-Tetramethylsuccinic acid, 97 is known for its stability and high purity, making it suitable for a wide range of applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 630-51-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 630-51:
(5*6)+(4*3)+(3*0)+(2*5)+(1*1)=53
53 % 10 = 3
So 630-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O4/c1-7(2,5(9)10)8(3,4)6(11)12/h1-4H3,(H,9,10)(H,11,12)

630-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-tetramethylbutanedioic acid

1.2 Other means of identification

Product number -
Other names Butanedioic acid,tetramethyl

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:630-51-3 SDS

630-51-3Relevant articles and documents

Reaction of Lithium Acylate α-Carbanions with Carbon Tetrachloride

Zorin,Zaynashev,Zorin

, p. 42 - 46 (2019/04/27)

Metalation of acetic, butanoic, or 2-methylpropanoic acid with lithium diisopropylamide in tetrahydrofuran under argon gave the corresponding lithium acylate α-carbanions which reacted with carbon tetrachloride at 20–25°C for 2 h to afford butanedioic acid or its 2,3-diethyl and 2,2,3,3-tetramethyl derivatives, as well as the corresponding α-chlorocarboxylic acids and chloroform. A radical mechanism was proposed for the formation of dicarboxylic and α-chlorocarboxylic acids.

Reactions of α-carbanions of lithium acylates with N,N-diethyl-N-chloro- and N,N-diethyl-N-bromoamines

Zorin,Zainashev,Zorin

, p. 2469 - 2472 (2016/12/24)

The interaction of α-carbanions of lithium acylates (prepared via metalation of acetic, butyric, or isobutyric acid with lithium diisopropylamide in tetrahydrofuran under argon atmosphere) with N,N-diethyl-N-chloro- or N,N-diethyl-N-bromoamine has resulte

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