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167010-30-2

(S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide is a chiral chemical compound with a molecular formula C12H12F2N2O3. It is a derivative of acetamide, featuring a phenyl ring with two fluorine atoms, an oxazolidinyl ring, and an acetamide group. (S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide may have potential pharmaceutical applications, but further research is needed to determine its specific properties and uses.

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  • 167010-30-2 Structure

  • Basic information

    1. Product Name: (S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide
    2. Synonyms: (S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide;(S)-N-((3-(3,5-Difluorophenyl)-2-oxooxazolidin-5-yl)Methyl)acetaMide
    3. CAS NO:167010-30-2
    4. Molecular Formula: C12H12F2N2O3
    5. Molecular Weight: 270.23
    6. EINECS: N/A
    7. Product Categories: pharmacetical
    8. Mol File: 167010-30-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 456.7°Cat760mmHg
    3. Flash Point: 230°C
    4. Appearance: /
    5. Density: 1.351g/cm3
    6. Vapor Pressure: 1.58E-08mmHg at 25°C
    7. Refractive Index: 1.523
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: (S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide(167010-30-2)
    12. EPA Substance Registry System: (S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide(167010-30-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 167010-30-2(Hazardous Substances Data)

167010-30-2 Usage

Uses

Used in Pharmaceutical Industry:
(S)-N-[[3-(3,5-Difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide is used as a potential pharmaceutical candidate for various applications due to its unique structure and chiral nature. Its specific properties and potential uses in drug development would require further research and investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 167010-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,0,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 167010-30:
(8*1)+(7*6)+(6*7)+(5*0)+(4*1)+(3*0)+(2*3)+(1*0)=102
102 % 10 = 2
So 167010-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12F2N2O3/c1-7(17)15-5-11-6-16(12(18)19-11)10-3-8(13)2-9(14)4-10/h2-4,11H,5-6H2,1H3,(H,15,17)/t11-/m0/s1

167010-30-2SDS

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 N-[[(5S)-3-(3,5-difluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-[[(5S)-3-(3,5-difluorophenyl)-2-oxo-5-oxazolidinyl]methyl]

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:167010-30-2 SDS

167010-30-2Relevant articles and documents

OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS

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Page/Page column 86, (2010/10/20)

The present invention relates to certain substituted phenyl oxazolidinones and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing the compounds of the present invention as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria, for example, multiple-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms, for example, Bacterioides spp. and Clostridia spp. species, and acid fast organisms, for example, Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.

Antibiotic oxazolidinone derivatives

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, (2008/06/13)

The invention concerns a compound of the formula (I): wherein, for example:T is of the formula (IA), (IB), or (IC); R1 is of the formula —NHC(=O)Rb wherein Rb is (1-4C)alkyl;R2 and R3 are hydrogen or

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