Cas 1357175-04-2,N-(cyclohexyl(2,7-dimethyl-1H-indol-3-yl)methyl)-4-methylbenzenesulfonamide

1357175-04-2

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Basic information

Product Name: N-(cyclohexyl(2,7-dimethyl-1H-indol-3-yl)methyl)-4-methylbenzenesulfonamide
Synonyms: N-(cyclohexyl(2,7-dimethyl-1H-indol-3-yl)methyl)-4-methylbenzenesulfonamide
CAS NO:1357175-04-2
Molecular Formula:
Molecular Weight: 410.58
EINECS: N/A
Product Categories: N/A
Mol File: 1357175-04-2.mol
Article Data: 1

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: N-(cyclohexyl(2,7-dimethyl-1H-indol-3-yl)methyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(cyclohexyl(2,7-dimethyl-1H-indol-3-yl)methyl)-4-methylbenzenesulfonamide(1357175-04-2)
EPA Substance Registry System: N-(cyclohexyl(2,7-dimethyl-1H-indol-3-yl)methyl)-4-methylbenzenesulfonamide(1357175-04-2)

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: 1357175-04-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357175-04-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,1,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1357175-04:
(9*1)+(8*3)+(7*5)+(6*7)+(5*1)+(4*7)+(3*5)+(2*0)+(1*4)=162
162 % 10 = 2
So 1357175-04-2 is a valid CAS Registry Number.

1357175-04-2Upstream product

1357175-04-2Downstream Products

1304141-65-8 (2R,3R)-(-)-2,7-dimethyl-3-(cyclohexylmethyl)indoline

1357175-04-2Relevant articles and documents

Pd-Catalyzed asymmetric hydrogenation of 3-(toluenesulfonamidoalkyl)indoles

Duan, Ying,Chen, Mu-Wang,Chen, Qing-An,Yu, Chang-Bin,Zhou, Yong-Gui

supporting information; experimental part, p. 1235 - 1238 (2012/03/07)

A series of 2-substituted 3-(toluenesulfonamidoalkyl)indoles was synthesized by application of (EtO)2POH or iodine as the catalyst, and was hydrogenated using chiral Pd catalyst, giving the 2,3-disubstituted indolines with up to 97% ee. The Royal Society of Chemistry 2012.

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