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

695192-70-2

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Basic information

Product Name: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole
Synonyms: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole
CAS NO:695192-70-2
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)-1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole(CAS DataBase Reference)
NIST Chemistry Reference: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole(695192-70-2)
EPA Substance Registry System: 9-bromo-4-nitro-2-(p-toluenesulfonyl)-1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole(695192-70-2)

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: 695192-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 695192-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,5,1,9 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 695192-70:
(8*6)+(7*9)+(6*5)+(5*1)+(4*9)+(3*2)+(2*7)+(1*0)=202
202 % 10 = 2
So 695192-70-2 is a valid CAS Registry Number.

695192-70-2Upstream product

695192-70-2Downstream Products

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

695192-70-2Relevant 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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