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117737-43-6

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117737-43-6 Usage

General Description

[(2-NITROPHENYL)SULFINYL]ACETIC ACID is a compound that consists of a nitrophenyl group attached to a sulfinyl functional group connected to an acetic acid moiety. It is a white to off-white crystalline solid that is used in organic chemistry and pharmaceutical research. The nitrophenyl group contributes to the compound's aromatic and electron-withdrawing properties, while the sulfinyl functional group provides a reactive center for chemical reactions. [(2-NITROPHENYL)SULFINYL]ACETIC ACID may be utilized as a reagent in the synthesis of various organic molecules, or it may have potential applications in the development of pharmaceutical compounds due to its unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 117737-43-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,3 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117737-43:
(8*1)+(7*1)+(6*7)+(5*7)+(4*3)+(3*7)+(2*4)+(1*3)=136
136 % 10 = 6
So 117737-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO5S/c10-8(11)5-15(14)7-4-2-1-3-6(7)9(12)13/h1-4H,5H2,(H,10,11)

117737-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2-NITROPHENYL)SULFINYL]ACETIC ACID

1.2 Other means of identification

Product number -
Other names IFLAB-BB F1304-0001

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:117737-43-6 SDS

117737-43-6Downstream Products

117737-43-6Relevant articles and documents

KINETICS AND MECHANISM OF OXIDATION OF (ARYLTHIO)ACETIC ACIDS BY PYRIDINIUM HYDROBROMIDE PERBROMIDE

Karunakaran, K.,Elango, K. P.

, p. 429 - 434 (2007/10/02)

Oxidation of several monosubstituted (phenylthio)acetic acids (PTAA) by pyridinium hydrobromide perbromide (PHPB) was studied in aqueous acetic acid.The reaction is first order with respect to PHPB.Michaelis-Menten type kinetics are observed with respect to (arylthio)acetic acid.The effect of solvent composition indicates that the transition state is more polar than the reactants.The formation constants of the intermediate substrate-PHPB complexes and the rates of their decomposition were determined at different temperatures.The rates of oxidation of para and meta-substituted (phenylthio)acetic acids were correlated with Hammett's substituent constants.The ρ value is -1.60 at 35 deg c.The rates of oxidation of ortho substituted compounds are correlated with Charton's triparametric equation.A mechanism involving the decomposition of the intermediate complex in the slow rate-determining step affording a sulphonium ion which hydrolyses in a subsequent fast step to the sulphoxide is proposed.

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