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(R)-N-((4-chlorophenyl)(2-hydroxynaphthalen-1-yl)methyl)-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1228803-06-2

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1228803-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228803-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,8,0 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1228803-06:
(9*1)+(8*2)+(7*2)+(6*8)+(5*8)+(4*0)+(3*3)+(2*0)+(1*6)=142
142 % 10 = 2
So 1228803-06-2 is a valid CAS Registry Number.

1228803-06-2Downstream Products

1228803-06-2Relevant academic research and scientific papers

Recyclable chiral dinuclear copper(II) complexes catalyzed asymmetric Friedel-Crafts alkylation of 1-naphthol using N-tosyl aldimine

Kumari, Prathibha,Jakhar, Ajay,Khan, Noor-Ul H.,Tak, Rajkumar,Kureshy, Rukhsana I.,Abdi, Sayed H.R.,Bajaj, Hari C.

, p. 138 - 142 (2015/06/25)

A highly efficient dinuclear copper complex catalyzed Friedel-Crafts reaction has been demonstrated for the alkylation of 1-naphthol using N-tosyl aldimine. In this context, various chiral amino alcohol derived Schiff base ligands with different achiral a

C3-Symmetric chiral trisimidazoline-catalyzed Friedel-Crafts (FC)-type reaction

Takizawa, Shinobu,Hirata, Shuichi,Murai, Kenichi,Fujioka, Hiromichi,Sasai, Hiroaki

supporting information, p. 5827 - 5830 (2014/08/05)

Imidazoline-catalyzed enantioselective Friedel-Crafts (FC)-type reactions were established using C3-symmetric chiral trisimidazolines. The imidazoline catalysts promoted the FC-type reaction of aldimines with 2-naphthols to produce the correspo

Organocatalytic enantioselective Friedel-Crafts reactions of 1-naphthols with aldimines

Liu, Guixia,Zhang, Shilei,Li, Hao,Zhang, Tangzhi,Wang, Wei

supporting information; experimental part, p. 828 - 831 (2011/04/26)

An organocatalytic enantioselective Friedel-Crafts reaction of 1-naphthols with aldimines has been developed. The method affords a direct access to chiral aminoarylnaphthols in good yields and with good to high enantioselectivities. (Figure Presented)

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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