Cas 127792-51-2,1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-3-ene-2-carboxylate

127792-51-2

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Basic information

Product Name: 1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-3-ene-2-carboxylate
Synonyms: 1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-3-ene-2-carboxylate
CAS NO:127792-51-2
Molecular Formula:
Molecular Weight: 405.472
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: 1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-3-ene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: 1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-3-ene-2-carboxylate(127792-51-2)
EPA Substance Registry System: 1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-3-ene-2-carboxylate(127792-51-2)

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: 127792-51-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127792-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,9 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 127792-51:
(8*1)+(7*2)+(6*7)+(5*7)+(4*9)+(3*2)+(2*5)+(1*1)=152
152 % 10 = 2
So 127792-51-2 is a valid CAS Registry Number.

127792-51-2Upstream product

127792-51-2Downstream Products

127792-62-5 1,1-dimethylethyl 3-<(benzoyloxy)methyl>-7α-methoxy-8-oxo-5-thia-1-azabicyclo<4.2.0>oct-2-ene-2-carboxylate 5,5-dioxide

127792-51-2Relevant academic research and scientific papers

Inhibition of human leukocyte elastase. 3. Synthesis and activity of 3'-substituted cephalosporins

Shah,Brause,Chandler,Finke,Ashe,Weston,Knight,Maycock,Doherty

, p. 2529 - 2535 (2007/10/02)

Several 3'-substituted cephalosporin sulfones were synthesized from 3-(hydroxymethyl)cephalosporin, which was prepared by Ti(OiPr)4 hydrolysis of the corresponding acetate. A method was also developed to prepare a 3-vinylcephalosporin. Some of

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