Cas 145576-98-3,(Z)-(3R,8R)-3-Benzoylamino-8-methyl-2-oxo-3,4,7,8-tetrahydro-2H-azocine-1-carboxylic acid benzyl ester

145576-98-3

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Basic information

Product Name: (Z)-(3R,8R)-3-Benzoylamino-8-methyl-2-oxo-3,4,7,8-tetrahydro-2H-azocine-1-carboxylic acid benzyl ester
Synonyms: (Z)-(3R,8R)-3-Benzoylamino-8-methyl-2-oxo-3,4,7,8-tetrahydro-2H-azocine-1-carboxylic acid benzyl ester
CAS NO:145576-98-3
Molecular Formula:
Molecular Weight: 392.455
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: (Z)-(3R,8R)-3-Benzoylamino-8-methyl-2-oxo-3,4,7,8-tetrahydro-2H-azocine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-(3R,8R)-3-Benzoylamino-8-methyl-2-oxo-3,4,7,8-tetrahydro-2H-azocine-1-carboxylic acid benzyl ester(145576-98-3)
EPA Substance Registry System: (Z)-(3R,8R)-3-Benzoylamino-8-methyl-2-oxo-3,4,7,8-tetrahydro-2H-azocine-1-carboxylic acid benzyl ester(145576-98-3)

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: 145576-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145576-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,5,7 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145576-98:
(8*1)+(7*4)+(6*5)+(5*5)+(4*7)+(3*6)+(2*9)+(1*8)=163
163 % 10 = 3
So 145576-98-3 is a valid CAS Registry Number.

145576-98-3Upstream product

145576-98-3Downstream Products

145576-99-4 N-((Z)-(3S,8S)-8-Methyl-2-oxo-1,2,3,4,7,8-hexahydro-azocin-3-yl)-benzamide

145576-98-3Relevant academic research and scientific papers

Regio- and Stereoselective Functionalisation of Monocyclic Medium Ring Lactams

Evans, P. Andrew,Collins, Ian,Hamley, Peter,Holmes, Andrew B.,Raithby, Paul R.,Russell, Keith

, p. 6859 - 6862 (2007/10/02)

The functionalisation of the potassium enolates of a series of racemic 7-, 8-, and 9-membered unsaturated lactams with trisyl azide and phenylselenyl chloride afforded the corresponding 3,n-disubstituted lactams with good stereoselectivities.

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