Cas 116459-04-2,1-[5-Nitro-6,9-bis-(toluene-4-sulfonyl)-tetrazolo[1,5-a]azepin-1-yl]-ethanone

116459-04-2

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Basic information

Product Name: 1-[5-Nitro-6,9-bis-(toluene-4-sulfonyl)-tetrazolo[1,5-a]azepin-1-yl]-ethanone
Synonyms:
CAS NO:116459-04-2
Molecular Formula:
Molecular Weight: 529.554
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-[5-Nitro-6,9-bis-(toluene-4-sulfonyl)-tetrazolo[1,5-a]azepin-1-yl]-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-[5-Nitro-6,9-bis-(toluene-4-sulfonyl)-tetrazolo[1,5-a]azepin-1-yl]-ethanone(116459-04-2)
EPA Substance Registry System: 1-[5-Nitro-6,9-bis-(toluene-4-sulfonyl)-tetrazolo[1,5-a]azepin-1-yl]-ethanone(116459-04-2)

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: 116459-04-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116459-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,5 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116459-04:
(8*1)+(7*1)+(6*6)+(5*4)+(4*5)+(3*9)+(2*0)+(1*4)=122
122 % 10 = 2
So 116459-04-2 is a valid CAS Registry Number.

116459-04-2Upstream product

53619-58-2 4-nitro-7-(p-tolylsulphonyl)benzofurazan N-oxide

116459-04-2Downstream Products

116459-04-2Relevant academic research and scientific papers

NUCLEOPHILIC ATTACK ON 4,7-DISUBSTITUTED BENZOFURAZANS AND THEIR N-OXIDES: SYNTHESIS OF TETRAZOLOAZEPINES

Belton, James G.,McElhinney, R Stanley

, p. 145 - 150 (2007/10/02)

The reaction of various nucleophiles with benzofurazans nd their N-oxides carrying electron-attracting substituents in the 4 and 7 positions has been reviewed and the study extended to include sulphonyl groups.As well as the simple replacement of leaving

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