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3-Methylsulfinylbenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90345-62-3

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90345-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90345-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90345-62:
(7*9)+(6*0)+(5*3)+(4*4)+(3*5)+(2*6)+(1*2)=123
123 % 10 = 3
So 90345-62-3 is a valid CAS Registry Number.

90345-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(methylsulfinyl)-Benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:90345-62-3 SDS

90345-62-3Downstream Products

90345-62-3Relevant academic research and scientific papers

Photodeoxygenation of dibenzothiophene S-oxide derivatives in aqueous media

Korang, James,Grither, Whitney R.,McCulla, Ryan D.

supporting information; experimental part, p. 4466 - 4476 (2010/06/13)

The use of atomic oxygen (O(3P)) as potent oxidant In water has suffered from the lack of a facile, efficient source. The photodeoxygenatlon of aromatic sulfoxides to the corresponding sulfides in organic solvents has been suggested to produce O(3P) in low quantum yields. The photolysis of 4,6-dihydroxymethyldibenzothiophene S-oxide and 2,8- dihydroxymethyldibenzothiophene S-oxide in water results in deoxygenation at significantly higher quantum yields than In organic solvents. Depending upon conditions, a variable amount of oxidation of the hydroxymethyl substituent into an aldehyde was observed to accompany deoxygenation. Analysis of the photoproducts Indicated the deoxygenation occurred by at least two different pH-sensitive mechanisms. Under basic conditions, photoinduced electron transfer yielding a hydroxysulfuranyl radical that decomposed by heterolytlc S-O cleavage was thermodynamically feasible. The thermodynamics of photoinduced electron transfer were expected to become increasingly unfavorable as the pH of the solution decreased. Thus, at neutral and acidic pH, an S-O bond scission mechanism was suspected. The observed increase In the photodeoxygenation quantum yields was consistent with charge separation accompanying S-O bond scission. Oxidative cleavage of alkenes In aerobic conditions suggested O(3P) was produced during photolysis In these conditions; however, the formation of discrete O-/HO may occur, particularly at low pH.

SULFOXIMINES AS KINASE INHIBITORS

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Page/Page column 96-97, (2008/12/05)

The present invention relates to organic molecules capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.

Asymmetric sulfoxidation catalyzed by a vanadium bromoperoxidase: Substrate requirements of the catalyst

Andersson, Malin A.,Allenmark, Stig G.

, p. 15293 - 15304 (2007/10/03)

An investigation of the catalytic effect of vanadium bromoperoxidase (VBrPO, from Corallina officinalis) on the oxidation of a series of prochiral sulfides by hydrogen peroxide, revealed that substrates having a cis- positioned carboxyl group are oxidized

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