Cas 86940-52-5,(6R,7R)-7-[2-Carboxy-2-(4-hydroxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid

86940-52-5

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Basic information

Product Name: (6R,7R)-7-[2-Carboxy-2-(4-hydroxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Synonyms: (6R,7R)-7-[2-Carboxy-2-(4-hydroxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS NO:86940-52-5
Molecular Formula:
Molecular Weight: 506.52
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: (6R,7R)-7-[2-Carboxy-2-(4-hydroxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (6R,7R)-7-[2-Carboxy-2-(4-hydroxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid(86940-52-5)
EPA Substance Registry System: (6R,7R)-7-[2-Carboxy-2-(4-hydroxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid(86940-52-5)

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: 86940-52-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86940-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,4 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86940-52:
(7*8)+(6*6)+(5*9)+(4*4)+(3*0)+(2*5)+(1*2)=165
165 % 10 = 5
So 86940-52-5 is a valid CAS Registry Number.

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86940-52-5Relevant academic research and scientific papers

Synthesis and Substituent Effects on Antibacterial Activity, Alkaline Hydrolysis Rates, and Infrared Absorption Frequencies of Some Cephem Analogues Related to Latamoxef (Moxalactam)

Narisada, Masayuki,Yoshida, Tadashi,Ohtani, Mitsuaki,Ezumi, Kiyoshi,Takasuka, Mamoru

, p. 1577 - 1582 (2007/10/02)

Relationships between intrinsic antibacterial activity and β-lactam reactivity of 7β-amino- and 7β-amino derivatives of 1-oxa- and 1-thiacephems, with or without the 7α-methoxy group (1-8), were investiga

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