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102653-81-6

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102653-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102653-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,5 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102653-81:
(8*1)+(7*0)+(6*2)+(5*6)+(4*5)+(3*3)+(2*8)+(1*1)=96
96 % 10 = 6
So 102653-81-6 is a valid CAS Registry Number.

102653-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(methylsulfinyl)benzoate

1.2 Other means of identification

Product number -
Other names 3-Methanesulfinyl-benzoic acid methyl ester

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:102653-81-6 SDS

102653-81-6Relevant articles and documents

Kinetics and mechanism of the oxidation of some organic sulfides by morpholinium chlorochromate

Malani, Neha,Baghmar, Manju,Sharma, Pradeep K.

, p. 65 - 72 (2009)

The oxidation of organic sulfides by morpholinium chlorochromate (MCC) resulted in the formation of the corresponding sulfoxides. The reaction is first order with respect to both MCC and the sulfide. The reaction is catalyzed by toluene-p-sulfonic acid (T

AZOLE-SUBSTITUTED PYRIDINE COMPOUND

-

Paragraph 0737; 0738, (2019/01/08)

The present invention provides a compound represented by formula [I'| shown below or a pharmaceutically acceptable salt thereof that has an inhibitory effect on 20-HETE producing enzyme, wherein the structure represented by formula [III] shown below represents any of the structures represented by formula group [IV] shown below, wherein R1 represents a hydrogen atom, a fluorine atom, methyl, etc.; R2, R3, and R4 each independently represent a hydrogen atom, a fluorine atom, or methyl; W represents a single bond, C1-3alkanediyl, or the formula -O-CH2CH2-; and ring A represents (a) substituted C4-6cycloalkyl, (b) substituted 4- to 6-membered saturated nitrogen-containing heterocyclyl, (c) substituted phenyl, (d) substituted pyridyl, (e) substituted 2,3-dihydrobenzofuran, (f) 4- to 6-membered saturated oxygen-containing heterocyclyl, etc.

Oxidation of organic sulfides by tetraethylammonium chlorochromate: A kinetic and mechanistic study

Sharma, Deepika,Pancharia,Vadera,Sharma, Pradeep K.

experimental part, p. 315 - 326 (2012/01/04)

The oxidation of organic sulfides by tetraethylammonium chlorochromate (TEACC) resulted in the formation of the corresponding sulfoxides. The reaction is first order with respect to both TEACC and the sulfide. The reaction is catalyzed by toluene-p-sulfon

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