Cas 141920-90-3,(3aS,8aR)-2,3-Diphenyl-2,3,3a,8a-tetrahydro-isoxazolo[5,4-c][1,2]diazepine-8-carboxylic acid ethyl ester

141920-90-3

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Basic information

Product Name: (3aS,8aR)-2,3-Diphenyl-2,3,3a,8a-tetrahydro-isoxazolo[5,4-c][1,2]diazepine-8-carboxylic acid ethyl ester
Synonyms:
CAS NO:141920-90-3
Molecular Formula:
Molecular Weight: 363.416
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: (3aS,8aR)-2,3-Diphenyl-2,3,3a,8a-tetrahydro-isoxazolo[5,4-c][1,2]diazepine-8-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,8aR)-2,3-Diphenyl-2,3,3a,8a-tetrahydro-isoxazolo[5,4-c][1,2]diazepine-8-carboxylic acid ethyl ester(141920-90-3)
EPA Substance Registry System: (3aS,8aR)-2,3-Diphenyl-2,3,3a,8a-tetrahydro-isoxazolo[5,4-c][1,2]diazepine-8-carboxylic acid ethyl ester(141920-90-3)

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: 141920-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141920-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,2 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141920-90:
(8*1)+(7*4)+(6*1)+(5*9)+(4*2)+(3*0)+(2*9)+(1*0)=113
113 % 10 = 3
So 141920-90-3 is a valid CAS Registry Number.

141920-90-3Upstream product

141920-90-3Downstream Products

141920-90-3Relevant academic research and scientific papers

REGIOSELECTIVE CYCLOADDITIONS OF 1H-AZEPINE AND 1H-1,2-DIAZEPINE DERIVATIVES WITH N,α-DIPHENYLNITRONE AND NITROSOBENZENE

Saito, Katsuhiro,Yoshino, Akihiro,Watanabe, Hiroyuki,Takahashi, Kensuke

, p. 497 - 504 (2007/10/02)

Reactions of 1-carbomethoxy-1H-azepine with N,α-diphenylnitrone afforded endo- and exo--type cycloadducts in almost the same ratio.Reactions of 1-carboethoxy-1H-azepine with nitrosobenzene in chloroform afforded - and -types of cycloadducts.Analogous results were obtained in the reactions using 1-carboethoxy-1H-1,2-diazepine.

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