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Benzeneethanesulfonic acid, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102834-59-3

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102834-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102834-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,3 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102834-59:
(8*1)+(7*0)+(6*2)+(5*8)+(4*3)+(3*4)+(2*5)+(1*9)=103
103 % 10 = 3
So 102834-59-3 is a valid CAS Registry Number.

102834-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-ethanesulfonic acid phenyl ester

1.2 Other means of identification

Product number -
Other names phenyl 2-phenylethanesulfonate

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:102834-59-3 SDS

102834-59-3Downstream Products

102834-59-3Relevant academic research and scientific papers

Unprecedented observation of sulfonamides in the transesterification of N-unsubstituted carbamates with sulfonyl chlorides

Dauvergne, Jér?me,Wellington, Kevin,Chibale, Kelly

, p. 43 - 47 (2007/10/03)

Sulfonamides have been identified as by-products in the base-mediated transesterification of N-unsubstituted carbamates with sulfonyl chlorides to give the corresponding sulfonates. A proposed mechanism and the synthesis of hindered 2,6-disubstituted arylsulfonates via this method are also reported.

KINETICS AND MECHANISM OF THE ALKALINE HYDROLYSIS OF SUBSTITUTED PHENYL PHENYLALKANE- AND PHENYLALKENESULFONATES

Vizgert, R. V.,Enya, V. I.

, p. 926 - 929 (2007/10/02)

The effect of the bond multiplicity and the distance between the aromatic ring and the sulfur atom of the sulfo group in a series of substituted phenyl benzene-, α-phenylmethane-, 2-phenylethane-, and 2-phenylethylenesulfonates on the kinetics and mechani

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