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Benzenesulfonamide, 4-methyl-N-[2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenylethyl]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62596-61-6

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62596-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62596-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,9 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62596-61:
(7*6)+(6*2)+(5*5)+(4*9)+(3*6)+(2*6)+(1*1)=146
146 % 10 = 6
So 62596-61-6 is a valid CAS Registry Number.

62596-61-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name toluene-4-sulfonic acid (R)-2-phenyl-2-(toluene-4-sulfonylamino)ethyl ester

1.2 Other means of identification

Product number -
Other names (R)-1-Phenyl-1-(toluol-4-sulfonylamino)-2-(toluol-4-sulfonyloxy)-aethan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62596-61-6 SDS

62596-61-6Relevant academic research and scientific papers

The importance of 1,2-anti-disubstitution in monotosylated diamine ligands for ruthenium(II)-catalysed asymmetric transfer hydrogenation

Hayes, Aidan,Clarkson, Guy,Wills, Martin

, p. 2079 - 2084 (2007/10/03)

The synthesis and applications to transfer hydrogenation of three derivatives of the popular TsDPEN are described. The results clearly demonstrate the importance of both disubstitution and the anti arrangement of substituents on this ligand. An explanatio

Influence of Phenylthio and Alkylthio Substituents on the Reactivity of 1-Oxa-1,3-butadienes in Hetero Diels-Alder Reactions

Tietze, Lutz F.,Fennen, Jens,Wichmann, Juergen

, p. 1507 - 1512 (2007/10/02)

The synthesis of the cyclic enamino ketones 1-3 bearing an alkylthio or an phenylthio group and their reactivity in hetero Diels-Alder reactions with enol ethers is described.Only compound 3 with an phenylthio group undergoes a cycloaddition with 16a-d to afford the diastereomeric adducts 17a-d and 18a-d.To estimate the activation by a phenylthio and alkylthio group semiempirical PM3/RHF calculations of the frontier orbital energies and coefficients of different enamine carbaldehydes have been performed.Key Words: Enamino ketones / 1,4-Thiazines / Hetero Diels-Alder reactions / Pyrans, dihydro / Calculations, semiempirical

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