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4372-15-0

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4372-15-0 Usage

General Description

Butan-2-ylpropanedioic acid, also known as diethylmalonic acid, is a compound with the chemical formula C9H16O4. It is an organic acid that is commonly used in organic synthesis and as a reagent in the production of pharmaceuticals and other organic compounds. The presence of a butyl group in the molecular structure of butan-2-ylpropanedioic acid makes it useful for its hydrophobic properties, which makes it suitable for use as a surfactant or emulsifier. Additionally, it is an important intermediate in the synthesis of various drugs and agrochemicals. Overall, butan-2-ylpropanedioic acid plays a significant role in the pharmaceutical and chemical industries due to its versatile properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4372-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4372-15:
(6*4)+(5*3)+(4*7)+(3*2)+(2*1)+(1*5)=80
80 % 10 = 0
So 4372-15-0 is a valid CAS Registry Number.

4372-15-0SDS

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 2-butan-2-ylpropanedioic acid

1.2 Other means of identification

Product number -
Other names sec-Butyl-malonsaeure

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:4372-15-0 SDS

4372-15-0Relevant articles and documents

Mesoionic Xanthine Analogues: Phosphodiesterase Inhibitory and Hypotensive Activity

Glennon, Richard A.,Rogers, Michael E.,Smith, J. Doyle,El-Said, M. K.,Egle, John L.

, p. 658 - 661 (2007/10/02)

Several mesoionic thiazolopyrimidines and mesoionic 1,3,4-thiadiazolopyrimidines were evaluated as inhibitors of cyclic-AMP phosphodiesterase.While small alkyl substituents at the 6 position have no significant effect on activity, phenyl and benzyl substituents enhance activity.Mesoionic structures such as 1 (R2 = H; R8 = Et) possess 20 to 40 times activity of theophylline when the R6 substituent is phenyl or 4-chlorobenzyl.Methyl and ethyl substitution at the 2 position essentially abolishes activity.Although plagued by solubility problems, several of the mesoionic derivatives were found to display weak hypotensive effects in vivo.

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