Cas 633282-90-3,9-bromo-4-nitro-2-(p-toluenesulfonyl)-2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indole

633282-90-3

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Basic information

Product Name: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indole
Synonyms: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indole
CAS NO:633282-90-3
Molecular Formula:
Molecular Weight: 499.341
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: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indole(CAS DataBase Reference)
NIST Chemistry Reference: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indole(633282-90-3)
EPA Substance Registry System: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indole(633282-90-3)

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: 633282-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 633282-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,3,2,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 633282-90:
(8*6)+(7*3)+(6*3)+(5*2)+(4*8)+(3*2)+(2*9)+(1*0)=153
153 % 10 = 3
So 633282-90-3 is a valid CAS Registry Number.

633282-90-3Upstream product

695192-70-2 9-bromo-4-nitro-2-(p-toluenesulfonyl)-1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole

633282-90-3Downstream Products

633282-90-3Relevant academic research and scientific papers

Preparation of peri-annulated indoles from polynitro compounds

Samet, Alexander V.,Yamskov, Alexei N.,Strelenko, Yuri A.,Semenov, Victor V.

experimental part, p. 6868 - 6872 (2009/12/06)

A novel peri-annulated heterocyclic system of 1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole was prepared starting from TNT via 4,6-dinitro-1-tosylindoline as a key intermediate. Base-induced C{double bond, long}C bond shift in 1,2-dihydrobenz[6,7]oxepino[4,

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