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107167-31-7

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107167-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107167-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107167-31:
(8*1)+(7*0)+(6*7)+(5*1)+(4*6)+(3*7)+(2*3)+(1*1)=107
107 % 10 = 7
So 107167-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O7/c1-5(13)11-6-4-17-12(9(6)15)19-10(16)7-2-3-8(14)18-7/h6-7H,2-4H2,1H3,(H,11,13)

107167-31-7SDS

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 (4-acetamido-3-oxo-1,2-oxazolidin-2-yl) 5-oxooxolane-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:107167-31-7 SDS

107167-31-7Related news

Synthesis of lactivicin (cas 107167-31-7) analogues08/12/2019

Aza analogues of lactivicin (1), a recently discovered novel antibiotic, were prepared by an application of our earlier convenient synthesis of 1 and its derivatives. A 1-unsubstituted pyrazolidinone derivative bearing 2-aminothiazol-4-yl-(Z)-methoxyiminoacetyl group exhibited in vitro antibacte...detailed

107167-31-7Relevant articles and documents

CHEMISTRY OF A NEW ANTIBIOTIC: LACTIVICIN

Harada, Setsuo,Tsubotani, Shigetoshi,Hida, Tsuneaki,Koyama, Katsuo,Kondo, Masahiro,Ono, Hideo

, p. 6589 - 6606 (2007/10/02)

A novel antibiotic, lactivicin (LTV), was isolated from the culture filtrates of two bacterial strains by various types of chromatography.LTV exists in aqueous solution as an equilibrium mixture of two epimers in a ratio of about 1:1.The chemical structure of LTV (C10H12N2O7) was determined to be 2-(4S-acetylamino-3-oxo-2-isoxazolidinyl)-5-oxo-tetrahydrofuran-2-carboxylic acid.The absolute configuration at the C-6 position was elucidated from the CD spectral data and X-ray crystallographic analysis of 4-amino-lactivinic acid obtained by the iminoether method.This compound is useful as a starting material for chemical modification.LTV showed antibacterial activity against Gram-positive and negative bacteria, susceptibility to β-lactamases, and affinity for penicillin-binding proteins.We therefore concluded that LTV is a novel skeleton antibiotic having β-lactam-like activities.

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