Cas 167111-32-2,benzyl (2R,R<sub>S</sub>)-1-(1-benzylcarbamoyl-2-methylprop-1-enyl)-4-oxoazetidine-2-sulfinamide

167111-32-2

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Basic information

Product Name: benzyl (2R,R_S)-1-(1-benzylcarbamoyl-2-methylprop-1-enyl)-4-oxoazetidine-2-sulfinamide
Synonyms: benzyl (2R,R_S)-1-(1-benzylcarbamoyl-2-methylprop-1-enyl)-4-oxoazetidine-2-sulfinamide
CAS NO:167111-32-2
Molecular Formula:
Molecular Weight: 411.525
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: benzyl (2R,R_S)-1-(1-benzylcarbamoyl-2-methylprop-1-enyl)-4-oxoazetidine-2-sulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: benzyl (2R,R_S)-1-(1-benzylcarbamoyl-2-methylprop-1-enyl)-4-oxoazetidine-2-sulfinamide(167111-32-2)
EPA Substance Registry System: benzyl (2R,R_S)-1-(1-benzylcarbamoyl-2-methylprop-1-enyl)-4-oxoazetidine-2-sulfinamide(167111-32-2)

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: 167111-32-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 167111-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,1,1 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 167111-32:
(8*1)+(7*6)+(6*7)+(5*1)+(4*1)+(3*1)+(2*3)+(1*2)=112
112 % 10 = 2
So 167111-32-2 is a valid CAS Registry Number.

167111-32-2Upstream product

167111-32-2Downstream Products

157087-75-7 (5S,6R)-4-benzyl-2-isopropylidene-5-oxo-5-thia-1,4-diazabicyclo<4.2.0>octane-3,8-dione

167111-32-2Relevant academic research and scientific papers

Functional derivatives of 4-oxoazetidine-2-sulfinic acids in asymmetric synthesis of 2-azacepham sulfoxides and their transformation

Herak, Jure J.,Vinkovic, Mladen,Lukic, Irena

, p. 5083 - 5092 (2007/10/02)

The enantiomerically pure 2-azacepham sulfoxide 2a was synthesized by stereocontrolled intramolecular cyclization of sulfinates 3 or sulfinamides 8 in the presence of dry hydrogen chloride followed by triethylamine. The cyclization accrued via equilibrate

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