Cas 141920-91-4,6-Oxa-2,3,7-triazabicyclo[3.2.2]nona-3,8-diene-2-carboxylic acid, 7-phenyl-, ethyl ester

141920-91-4

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Basic information

Product Name: 6-Oxa-2,3,7-triazabicyclo[3.2.2]nona-3,8-diene-2-carboxylic acid, 7-phenyl-, ethyl ester
Synonyms:
CAS NO:141920-91-4
Molecular Formula: C14H15N3O3
Molecular Weight: 273.291
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: 6-Oxa-2,3,7-triazabicyclo[3.2.2]nona-3,8-diene-2-carboxylic acid, 7-phenyl-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-Oxa-2,3,7-triazabicyclo[3.2.2]nona-3,8-diene-2-carboxylic acid, 7-phenyl-, ethyl ester(141920-91-4)
EPA Substance Registry System: 6-Oxa-2,3,7-triazabicyclo[3.2.2]nona-3,8-diene-2-carboxylic acid, 7-phenyl-, ethyl ester(141920-91-4)

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: 141920-91-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141920-91-4 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 141920-91:
(8*1)+(7*4)+(6*1)+(5*9)+(4*2)+(3*0)+(2*9)+(1*1)=114
114 % 10 = 4
So 141920-91-4 is a valid CAS Registry Number.

141920-91-4Upstream product

141920-91-4Downstream Products

141920-91-4Relevant 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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