Cas 853796-30-2,Acetamide, N-[[(5S)-3-[3-fluoro-4-(1-thia-4,8-diazaspiro[4.5]dec-8-yl)phenyl]-2-oxo- 5-oxazolidinyl]methyl]-

853796-30-2

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Basic information

Product Name: Acetamide, N-[[(5S)-3-[3-fluoro-4-(1-thia-4,8-diazaspiro[4.5]dec-8-yl)phenyl]-2-oxo- 5-oxazolidinyl]methyl]-
Synonyms:
CAS NO:853796-30-2
Molecular Formula: C19H25FN4O3S
Molecular Weight: 408.497
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: Acetamide, N-[[(5S)-3-[3-fluoro-4-(1-thia-4,8-diazaspiro[4.5]dec-8-yl)phenyl]-2-oxo- 5-oxazolidinyl]methyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, N-[[(5S)-3-[3-fluoro-4-(1-thia-4,8-diazaspiro[4.5]dec-8-yl)phenyl]-2-oxo- 5-oxazolidinyl]methyl]-(853796-30-2)
EPA Substance Registry System: Acetamide, N-[[(5S)-3-[3-fluoro-4-(1-thia-4,8-diazaspiro[4.5]dec-8-yl)phenyl]-2-oxo- 5-oxazolidinyl]methyl]-(853796-30-2)

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: 853796-30-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 853796-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,7,9 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 853796-30:
(8*8)+(7*5)+(6*3)+(5*7)+(4*9)+(3*6)+(2*3)+(1*0)=212
212 % 10 = 2
So 853796-30-2 is a valid CAS Registry Number.

853796-30-2Upstream product

853796-30-2Downstream Products

853796-30-2Relevant academic research and scientific papers

SUBSTITUTED PIPERIDINO PHENYLOXAZOLIDINONES HAVING ANTIMICRIOBIAL ACTIVITY WITH IMPROVED IN VIVO EFFICACY

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Page/Page column 105, (2010/02/12)

The present invention provides agents having antimicrobial activity for preventing and treating infectious diseases. Thus, the present invention provides novel substituted piperidino phenyloxazolidinone derivatives, processes for making compounds as well as antimicrobial compositions containing said derivatives as active ingredients and methods of treating bacterial infections with the said derivatives.

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