Cas 872690-19-2,2-[1-(4-bromo-phenyl)-3-oxo-2,3,4,5-tetrahydro-1<i>H</i>-benzo[<i>c</i>]azepin-4-yl]-isoindole-1,3-dione

872690-19-2

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Basic information

Product Name: 2-[1-(4-bromo-phenyl)-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl]-isoindole-1,3-dione
Synonyms: 2-[1-(4-bromo-phenyl)-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl]-isoindole-1,3-dione
CAS NO:872690-19-2
Molecular Formula:
Molecular Weight: 461.315
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-[1-(4-bromo-phenyl)-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl]-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-[1-(4-bromo-phenyl)-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl]-isoindole-1,3-dione(872690-19-2)
EPA Substance Registry System: 2-[1-(4-bromo-phenyl)-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl]-isoindole-1,3-dione(872690-19-2)

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: 872690-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872690-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,6,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 872690-19:
(8*8)+(7*7)+(6*2)+(5*6)+(4*9)+(3*0)+(2*1)+(1*9)=202
202 % 10 = 2
So 872690-19-2 is a valid CAS Registry Number.

872690-19-2Upstream product

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872690-19-2Relevant academic research and scientific papers

Synthesis of substituted 4-amino-2-benzazepin-3-ones via N-acyliminium ion cyclizations

Ballet, Steven,Urbanczyk-Lipkowska, Zofia,Tourwé, Dirk

, p. 2791 - 2795 (2007/10/03)

Two versatile syntheses of 1- and 1,2-disubstituted 2-benzazepinones are presented, using N-acyliminium ions as reactive intermediates. The methodology for 1-substitution is based on the synthesis of benzotriazole adducts, which are cyclized upon addition

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