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4'-Hydroxy-m-phenoxy benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35065-12-4

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35065-12-4 Usage

Uses

A metabolite of pyrethroid insecticides such as: Deltamethrin,

Check Digit Verification of cas no

The CAS Registry Mumber 35065-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,6 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35065-12:
(7*3)+(6*5)+(5*0)+(4*6)+(3*5)+(2*1)+(1*2)=94
94 % 10 = 4
So 35065-12-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O4/c14-10-4-6-11(7-5-10)17-12-3-1-2-9(8-12)13(15)16/h1-8,14H,(H,15,16)

35065-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4'-Hydroxy)phenoxybenzoic Acid

1.2 Other means of identification

Product number -
Other names 3-(4-hydroxyphenoxy)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:35065-12-4 SDS

35065-12-4Relevant academic research and scientific papers

Intermediates for leukotriene antagonists

-

, (2008/06/13)

This invention provides benzene derivatives which are leukotriene antagonists, formulations of those derivatives, intermediates for preparing the derivatives, and a method of using those derivatives for the treatment of conditions characterized by an excessive release of leukotrienes.

Benzophenone Dicarboxylic Acid Antagonists of Leukotriene B4. 1. Structure-Activity Relationships of the Benzophenone Nucleus

Gapinski, D. Mark,Mallett, Barbara E.,Froelich, Larry L.,Jackson, William T.

, p. 2798 - 2807 (2007/10/02)

A series of lipophilic benzophenone dicarboxylic acid derivatives was prepared which inhibited the binding of the potent chemotaxin leukotriene B4 to its receptor(s) on intact human neutrophils.With a radioligand-binding assay as a measure of receptor affinity, a structure-activity relationship for this series was investigated.Both acidic residues were required for receptor-binding activity.The relative orientation of the two acidic groups was important for optimal binding.Replacement of the carbonyl group of the benzophenone with a variety of polar and nonpolar linking groups lead to only small changes in binding affinity, indicating the linking group may not be involved in receptor recognition.Further structure-activity relationships within this series are reported in an accompanying paper.

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