Cas 1289014-62-5,(R)-N-((2-fluorophenyl)(2-hydroxynaphthalen-1-yl)methyl)-4-methylbenzenesulfonamide

1289014-62-5

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Basic information

Product Name: (R)-N-((2-fluorophenyl)(2-hydroxynaphthalen-1-yl)methyl)-4-methylbenzenesulfonamide
Synonyms:
CAS NO:1289014-62-5
Molecular Formula:
Molecular Weight: 421.492
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: (R)-N-((2-fluorophenyl)(2-hydroxynaphthalen-1-yl)methyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-((2-fluorophenyl)(2-hydroxynaphthalen-1-yl)methyl)-4-methylbenzenesulfonamide(1289014-62-5)
EPA Substance Registry System: (R)-N-((2-fluorophenyl)(2-hydroxynaphthalen-1-yl)methyl)-4-methylbenzenesulfonamide(1289014-62-5)

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: 1289014-62-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1289014-62-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,9,0,1 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1289014-62:
(9*1)+(8*2)+(7*8)+(6*9)+(5*0)+(4*1)+(3*4)+(2*6)+(1*2)=165
165 % 10 = 5
So 1289014-62-5 is a valid CAS Registry Number.

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1289014-62-5Relevant academic research and scientific papers

Asymmetric aza-friedel-crafts reaction of 2-naphthol with tosylimines catalyzed by a dinuclear zinc complex

Niu, Liang-Feng,Xin, Yang-Chun,Wang, Ren-Lin,Jiang, Fan,Xu, Peng-Fei,Hui, Xin-Ping

supporting information; experimental part, p. 765 - 768 (2010/06/14)

The first asymmetric aza-Friedel-Crafts reaction of 2-naphthol with tosylimines was developed via a dinuclear zinc catalyst (up to 98% ee). It provided a new method for the asymmetric synthesis of Betti base derivatives.

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