Cas 738626-29-4,(+)-N-{4-chlorophenyl-[2-(trimethylsilyl)phenyl]methyl}-4-methylbenzenesulfonamide

738626-29-4

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Basic information

Product Name: (+)-N-{4-chlorophenyl-[2-(trimethylsilyl)phenyl]methyl}-4-methylbenzenesulfonamide
Synonyms: (+)-N-{4-chlorophenyl-[2-(trimethylsilyl)phenyl]methyl}-4-methylbenzenesulfonamide
CAS NO:738626-29-4
Molecular Formula:
Molecular Weight: 444.069
EINECS: N/A
Product Categories: N/A
Mol File: 738626-29-4.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-{4-chlorophenyl-[2-(trimethylsilyl)phenyl]methyl}-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (+)-N-{4-chlorophenyl-[2-(trimethylsilyl)phenyl]methyl}-4-methylbenzenesulfonamide(738626-29-4)
EPA Substance Registry System: (+)-N-{4-chlorophenyl-[2-(trimethylsilyl)phenyl]methyl}-4-methylbenzenesulfonamide(738626-29-4)

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: 738626-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 738626-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,8,6,2 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 738626-29:
(8*7)+(7*3)+(6*8)+(5*6)+(4*2)+(3*6)+(2*2)+(1*9)=194
194 % 10 = 4
So 738626-29-4 is a valid CAS Registry Number.

738626-29-4Upstream product

738626-29-4Downstream Products

738626-29-4Relevant articles and documents

N-Boc-L-valine-connected amidomonophosphane rhodium(I) catalyst for asymmetric arylation of N-tosylarylimines with arylboroxines

Kuriyama, Masami,Soeta, Takahiro,Hao, Xinyu,Chen, Qian,Tomioka, Kiyoshi

, p. 8128 - 8129 (2007/10/03)

A catalytic asymmetric arylation of sterically tuned imines with arylboroxines was developed by using N-Boc-L-valine-connected amidomonophosphane rhodium(I) catalyst in n-PrOH. The TMS group used for the steric tuning of imines is convertible to other fun

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