Cas 945933-25-5,(E)-N-(1-cyclohexyl-2-methyl-but-2-enyl)-4-methyl-benzenesulfonamide

945933-25-5

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Basic information

Product Name: (E)-N-(1-cyclohexyl-2-methyl-but-2-enyl)-4-methyl-benzenesulfonamide
Synonyms: (E)-N-(1-cyclohexyl-2-methyl-but-2-enyl)-4-methyl-benzenesulfonamide
CAS NO:945933-25-5
Molecular Formula:
Molecular Weight: 321.484
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-(1-cyclohexyl-2-methyl-but-2-enyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N-(1-cyclohexyl-2-methyl-but-2-enyl)-4-methyl-benzenesulfonamide(945933-25-5)
EPA Substance Registry System: (E)-N-(1-cyclohexyl-2-methyl-but-2-enyl)-4-methyl-benzenesulfonamide(945933-25-5)

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: 945933-25-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945933-25-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,9,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 945933-25:
(8*9)+(7*4)+(6*5)+(5*9)+(4*3)+(3*3)+(2*2)+(1*5)=205
205 % 10 = 5
So 945933-25-5 is a valid CAS Registry Number.

945933-25-5Upstream product

945933-25-5Downstream Products

945933-25-5Relevant academic research and scientific papers

Allylic amines via iridium-catalyzed C-C bond forming hydrogenation: Imine vinylation in the absence of stoichiometric byproducts or metallic reagents

Barchuk, Andriy,Ngai, Ming-Yu,Krische, Michael J.

, p. 8432 - 8433 (2007)

Exposure of aromatic, heteroaromatic, and aliphatic N-arylsulfonyl aldimines 1a-12a in toluene solution at 60 °C to 2-butyne and hydrogen at ambient pressure in the presence of a cationic iridium(I) catalyst modified by BIPHEP enables formation of reducti

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