Cas 123201-60-5,(2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester

123201-60-5

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Basic information

Product Name: (2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester
Synonyms: (2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester
CAS NO:123201-60-5
Molecular Formula:
Molecular Weight: 479.189
EINECS: N/A
Product Categories: N/A
Mol File: 123201-60-5.mol
Article Data: 1

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: (2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester(123201-60-5)
EPA Substance Registry System: (2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester(123201-60-5)

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: 123201-60-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123201-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,0 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123201-60:
(8*1)+(7*2)+(6*3)+(5*2)+(4*0)+(3*1)+(2*6)+(1*0)=65
65 % 10 = 5
So 123201-60-5 is a valid CAS Registry Number.

123201-60-5Upstream product

123201-60-5Downstream Products

123201-60-5Relevant articles and documents

REACTIVITY PARAMETERS OF THE METAL ASSISTED 1,2-CLEAVAGE OF PENICILLINS

Alpegiani, Marco,Bodeschi, Angelo,Bissolino, Pierluigi,Visentin, Giuseppina,Zarini, Franco,et al.

, p. 617 - 628 (2007/10/02)

A straightforward and smooth conversion of penicillins into 1,2-secopenicillanates is described.The thiazolidine ring opening is brought about by the co-operative effect of strong non-nucleophilic bases and thiophilic heavy metal salts.The nature of the l

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