Cas 1584667-89-9,(E)-N,N'-(5-fluoro-2-((4-fluorophenyl)diazenyl)-1,3-phenylene)bis(4-nitrobenzenesulfonamide)

1584667-89-9

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Basic information

Product Name: (E)-N,N'-(5-fluoro-2-((4-fluorophenyl)diazenyl)-1,3-phenylene)bis(4-nitrobenzenesulfonamide)
Synonyms: (E)-N,N'-(5-fluoro-2-((4-fluorophenyl)diazenyl)-1,3-phenylene)bis(4-nitrobenzenesulfonamide)
CAS NO:1584667-89-9
Molecular Formula:
Molecular Weight: 618.555
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: (E)-N,N'-(5-fluoro-2-((4-fluorophenyl)diazenyl)-1,3-phenylene)bis(4-nitrobenzenesulfonamide)(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N,N'-(5-fluoro-2-((4-fluorophenyl)diazenyl)-1,3-phenylene)bis(4-nitrobenzenesulfonamide)(1584667-89-9)
EPA Substance Registry System: (E)-N,N'-(5-fluoro-2-((4-fluorophenyl)diazenyl)-1,3-phenylene)bis(4-nitrobenzenesulfonamide)(1584667-89-9)

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: 1584667-89-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1584667-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,4,6,6 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1584667-89:
(9*1)+(8*5)+(7*8)+(6*4)+(5*6)+(4*6)+(3*7)+(2*8)+(1*9)=229
229 % 10 = 9
So 1584667-89-9 is a valid CAS Registry Number.

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1584667-89-9Relevant academic research and scientific papers

Rhodium-catalyzed direct ortho C-N bond formation of aromatic Azo compounds with azides

Wang, Hao,Yu, Yang,Hong, Xiaohu,Tan, Qitao,Xu, Bin

, p. 3279 - 3288 (2014/05/06)

An efficient rhodium-catalyzed regioselective C-N bond formation of azo compounds in good to excellent yields through C-H bond functionalization using azides as the nitrogen source was developed. Alkyl, aryl, and sulfonyl azides could be efficiently assem

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