Cas 131111-01-8,2-[(S)-2-Allyl-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-3-methyl-but-2-enoic acid methyl ester

131111-01-8

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Basic information

Product Name: 2-[(S)-2-Allyl-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-3-methyl-but-2-enoic acid methyl ester
Synonyms:
CAS NO:131111-01-8
Molecular Formula:
Molecular Weight: 372.421
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: 2-[(S)-2-Allyl-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-3-methyl-but-2-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(S)-2-Allyl-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-3-methyl-but-2-enoic acid methyl ester(131111-01-8)
EPA Substance Registry System: 2-[(S)-2-Allyl-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-3-methyl-but-2-enoic acid methyl ester(131111-01-8)

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: 131111-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131111-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,1 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131111-01:
(8*1)+(7*3)+(6*1)+(5*1)+(4*1)+(3*1)+(2*0)+(1*1)=48
48 % 10 = 8
So 131111-01-8 is a valid CAS Registry Number.

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131111-01-8Relevant academic research and scientific papers

Allyltin reagents. A general approach to carbon-carbon bond formation applied to penicillin derived azetidinones - I

Blaszczak, Larry C.,Armour, H. Kenneth,Halligan, Noreen G.

, p. 5693 - 5696 (1990)

Allyltributyltin has been shown to be a useful reagent for allyl transfer to penicillin derived azetidinones. The radical mechanism of the reaction has been demonstrated and its stereochemical consequences recorded. The process opens new possibilities for

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