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198021-38-4

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198021-38-4 Usage

Usage

Antibacterial agent

Specific application

Treatment of skin and soft tissue infections caused by Gram-positive bacteria

Mechanism of action

Inhibits protein synthesis in bacteria, preventing growth and reproduction

Administration route

Oral, well-absorbed

Potential issues

Side effects, interactions with other medications, and development of antibiotic resistance

Importance

Valuable alternative for treating bacterial infections

Check Digit Verification of cas no

The CAS Registry Mumber 198021-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,0,2 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 198021-38:
(8*1)+(7*9)+(6*8)+(5*0)+(4*2)+(3*1)+(2*3)+(1*8)=144
144 % 10 = 4
So 198021-38-4 is a valid CAS Registry Number.

198021-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4S,5R)-2-oxo-4,5-diphenyl-1,3-oxazolidin-3-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 2-((4S,5R)-2-Oxo-4,5-diphenyloxazolidin-3-yl)acetic acid

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:198021-38-4 SDS

198021-38-4Relevant articles and documents

A practical synthesis of enantiopure 4,4,4-trifluoro-allo-threonine from an easily available fluorinated building block

Cho, Joonil,Irie, Siho,Iwahashi, Nobutaka,Itoh, Yoshimitsu,Saigo, Kazuhiko,Ishida, Yasuhiro

, p. 127 - 131 (2015/02/02)

A practical method to prepare enantiopure 4,4,4-trifluoro-allo-threonine was developed by using an easily available fluorinated building block and a chiral auxiliary as starting materials. Trifluoroacetic anhydride was annulated with a ketene, derived fro

CARBACEPHEM β-LACTAM ANTIBIOTICS

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Page/Page column 62, (2010/04/06)

Carbacephem -lactam antibiotics having structure (I) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar1, Ar2, R1 and R2 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

CARBACEPHEM β-LACTAM ANTIBIOTICS

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Page/Page column 75-76, (2009/05/30)

Carbacephem β-lactam antibiotics having the following chemical structures (I) and (II) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, R1, R2 and R3 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

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