Cas 1605321-83-2,3,8-di(4-cyanophenoxy)-1,10-bis-(3-nitrobenzenesulfonylimino)deca-2,4,6,8-tetraene-2,9-disulfonamide

1605321-83-2

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Basic information

Product Name: 3,8-di(4-cyanophenoxy)-1,10-bis-(3-nitrobenzenesulfonylimino)deca-2,4,6,8-tetraene-2,9-disulfonamide
Synonyms:
CAS NO:1605321-83-2
Molecular Formula:
Molecular Weight: 922.912
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: 3,8-di(4-cyanophenoxy)-1,10-bis-(3-nitrobenzenesulfonylimino)deca-2,4,6,8-tetraene-2,9-disulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 3,8-di(4-cyanophenoxy)-1,10-bis-(3-nitrobenzenesulfonylimino)deca-2,4,6,8-tetraene-2,9-disulfonamide(1605321-83-2)
EPA Substance Registry System: 3,8-di(4-cyanophenoxy)-1,10-bis-(3-nitrobenzenesulfonylimino)deca-2,4,6,8-tetraene-2,9-disulfonamide(1605321-83-2)

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: 1605321-83-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1605321-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,5,3,2 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1605321-83:
(9*1)+(8*6)+(7*0)+(6*5)+(5*3)+(4*2)+(3*1)+(2*8)+(1*3)=132
132 % 10 = 2
So 1605321-83-2 is a valid CAS Registry Number.

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1605321-83-2Relevant academic research and scientific papers

On the reaction products of 4-substituted 3-pyridinesulfonamides with some benzenesulfonyl chloride derivatives

Brzozowski, Zdzislaw,Slawinski, Jaroslaw,Szafranski, Krzysztof

, p. 11 - 17 (2014/02/14)

The reactions of 4-substituted 3-pyridinesulfonamides 1a, 1b, 1c, 1d, 1e with benzenesulfonyl chlorides 2a, 2b, 2c, 2d, 2e, 2f in acetonitrile were investigated. Depending on the structure of arylsulfonyl chlorides and the reaction conditions the followin

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