Cas 872690-27-2,[1-(4-bromo-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-1,3,4,5-tetrahydro-benzo[<i>c</i>]azepin-2-yl]-acetic acid ethyl ester

872690-27-2

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Basic information

Product Name: [1-(4-bromo-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-1,3,4,5-tetrahydro-benzo[c]azepin-2-yl]-acetic acid ethyl ester
Synonyms: [1-(4-bromo-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-1,3,4,5-tetrahydro-benzo[c]azepin-2-yl]-acetic acid ethyl ester
CAS NO:872690-27-2
Molecular Formula:
Molecular Weight: 547.405
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: [1-(4-bromo-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-1,3,4,5-tetrahydro-benzo[c]azepin-2-yl]-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-(4-bromo-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-1,3,4,5-tetrahydro-benzo[c]azepin-2-yl]-acetic acid ethyl ester(872690-27-2)
EPA Substance Registry System: [1-(4-bromo-phenyl)-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-oxo-1,3,4,5-tetrahydro-benzo[c]azepin-2-yl]-acetic acid ethyl ester(872690-27-2)

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: 872690-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872690-27-2 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 872690-27:
(8*8)+(7*7)+(6*2)+(5*6)+(4*9)+(3*0)+(2*2)+(1*7)=202
202 % 10 = 2
So 872690-27-2 is a valid CAS Registry Number.

872690-27-2Upstream product

872690-27-2Downstream Products

872690-27-2Relevant 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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