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88382-49-4

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88382-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88382-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88382-49:
(7*8)+(6*8)+(5*3)+(4*8)+(3*2)+(2*4)+(1*9)=174
174 % 10 = 4
So 88382-49-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O2S/c15-14(16)12-8-6-11(7-9-12)10-17-13-4-2-1-3-5-13/h1-9H,10H2,(H,15,16)

88382-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(PHENYLTHIO)METHYL]BENZOIC ACID

1.2 Other means of identification

Product number -
Other names p-<(phenylthio)methyl>benzoic acid

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:88382-49-4 SDS

88382-49-4Relevant articles and documents

ARYLSULFANYL COMPOUNDS AND COMPOSITIONS FOR DELIVERING ACTIVE AGENTS

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Page/Page column 58-59, (2008/06/13)

Compounds and compositions for the delivery of active agents are provided. Methods of administration and preparation are also provided.

Kinetics of the reaction of sodium arylthiolates with nitro-carboxybenzyl halide derivatives

Hamed, Ezzat A.,El-Bardan, Ali A.,El-Mallah, Nabila M.

, p. 283 - 289 (2007/10/03)

The rate constants for the reactions of 4-halomethyl-3-nitrobenzoic acids, the nonnitro derivatives, and their ethyl esters with arylthiolates were measured at different temperatures. It was found that the retardation in rate constants compared to benzyl halides is due to the electrostatic repulsion between the electronegative substituents (COO- and/or NO2) in the substrates and thiolate ions Good correlations between log K2 values of the acids and carbon basicities of thiolates were found while log k2 values of the esters show good straight lines with Hammett a constants, pKa. and carbon basicities of arylthiolates.

Synthesis and antifolate properties of 10-alkyl-8,10-dideazaminopterins

DeGraw,Christie,Brown,Kelly,Kisliuk,Gaumont,Sirotnak

, p. 376 - 380 (2007/10/02)

The synthesis of 10-alkyl analogues of the potent antitumor agent 8,10-dideazaminopterin is described. Alkylation of appropriate α-alkyl homoterephthalate esters with 2,4-diamino-6-(bromomethyl)-8-deazapteridine afforded 10-alkyl-10-carboxy-4-amino-4-deox

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