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41480-00-6

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41480-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41480-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,8 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41480-00:
(7*4)+(6*1)+(5*4)+(4*8)+(3*0)+(2*0)+(1*0)=86
86 % 10 = 6
So 41480-00-6 is a valid CAS Registry Number.

41480-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl 2,4-dimethylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-benzolsulfonsaeure-phenylester

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:41480-00-6 SDS

41480-00-6Downstream Products

41480-00-6Relevant articles and documents

The effects of the reaction conditions on the metalation of phenyl p- Toluenesulfonate (Phenyl Tosylate)

Kimachi, Tetsutaro

, p. 139 - 141 (2007/10/03)

Directed ortho metalation of phenyl p-toluenesulfonate (phenyl tosylate) was carried out and the reaction was found to be controlled by the conditions (base, solvent, temperature, with or without ligand) to some extent.

CATALYTIC SULFONYLATION OF PHENOL BY STERICALLY HINDERED SULFONYL CHLORIDES

Vizgert, R.V.,Maksimenko, N.N.,Rubleva, L.I.

, p. 2144 - 2146 (2007/10/02)

The sulfonylation of phenol by substituted arenesulfonyl chlorides XArSO2Cl in the presence of triethylamine in benzene was studied by potentiometric titration.A linear relation was obtained between the logaritmhs of the catalytic rate constants and the steric constants Eso of the substituents in the sulfonyl chloride.The contribution from the induction and steric effects of the substituents at position2 to the kinetics of the process was assessed.It was concluded that the steric effect plays a predominant role over the induction and resonance effects.

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