Cas 1160366-86-8,(S)-N-[[3-[3-fluoro-4-[4-[2-(4-nitrobenzamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide

1160366-86-8

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Basic information

Product Name: (S)-N-[[3-[3-fluoro-4-[4-[2-(4-nitrobenzamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide
Synonyms:
CAS NO:1160366-86-8
Molecular Formula:
Molecular Weight: 542.524
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-N-[[3-[3-fluoro-4-[4-[2-(4-nitrobenzamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-[[3-[3-fluoro-4-[4-[2-(4-nitrobenzamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide(1160366-86-8)
EPA Substance Registry System: (S)-N-[[3-[3-fluoro-4-[4-[2-(4-nitrobenzamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide(1160366-86-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1160366-86-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160366-86-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,3,6 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1160366-86:
(9*1)+(8*1)+(7*6)+(6*0)+(5*3)+(4*6)+(3*6)+(2*8)+(1*6)=138
138 % 10 = 8
So 1160366-86-8 is a valid CAS Registry Number.

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1160366-86-8Relevant academic research and scientific papers

Synthesis and antibacterial activities of eperezolid analogs with glycinyl substitutions

Wang, Xiao-Jun,Wu, Ning,Du, Guang-Jian,Zhao, Shuang-Qi,Yan, Ming,Gu, Lian-Quan

experimental part, p. 377 - 385 (2009/10/23)

A series of eperezolid analogs with glycinyl substitutions were prepared and their antibacterial activities were studied against a panel of susceptible and resistant Gram-positive bacteria. The compounds with N-arylacyl or N-heteroarylacyl glycinyl struct

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