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80079-49-8

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80079-49-8 Usage

General Description

1-(2-methyl-1-oxoallyl)-5-oxo-L-proline is a chemical compound that belongs to the class of organic compounds known as pyrrolidine carboxylic acids. It has a molecular formula of C8H11NO4 and a molecular weight of 189.17 g/mol. 1-(2-methyl-1-oxoallyl)-5-oxo-L-proline is derived from proline, an amino acid, and is involved in the biosynthesis of the essential amino acid, L-proline. It is commonly used as a building block in the synthesis of various pharmaceuticals and natural products. Additionally, 1-(2-methyl-1-oxoallyl)-5-oxo-L-proline has been studied for its potential biological activities, including anti-inflammatory and anti-cancer properties.

Check Digit Verification of cas no

The CAS Registry Mumber 80079-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,7 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80079-49:
(7*8)+(6*0)+(5*0)+(4*7)+(3*9)+(2*4)+(1*9)=128
128 % 10 = 8
So 80079-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO4/c1-5(2)8(12)10-6(9(13)14)3-4-7(10)11/h6H,1,3-4H2,2H3,(H,13,14)/t6-/m0/s1

80079-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-(2-methylprop-2-enoyl)-5-oxopyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names EINECS 279-390-1

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:80079-49-8 SDS

80079-49-8Downstream Products

80079-49-8Relevant articles and documents

A Convenient Preparation of N-Acylpyroglutamic Acid

Imaki, Katsuhiro,Niwa, Haruki,Sakuyama, Shigeru,Okada, Takanori,Toda, Masaaki,Hayashi, Masaki

, p. 2699 - 2701 (2007/10/02)

Pyroglutamic acid reacted with acyl chloride in the presence of triethylamine in acetonitrile, yielding N-acylpyroglutamic acid without epimerization by way of mixed anhydride formation followed by intramolecular N-acylation.Keywords - angiotensin-converting enzyme; pyroglutamic acid; N-acylpyroglutamic acid; (2S)-1-pyroglutamic acid; N-acetyl-L-pyroglutamic acid

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