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2-(2-Hydroxyphenoxy)benzoic acid, also known as salicylic acid phenol ester, is a white crystalline solid with the chemical formula C13H10O4. It is an organic compound derived from salicylic acid and phenol, featuring a benzoic acid group and a hydroxyphenoxy group. 2-(2-Hydroxyphenoxy)benzoic acid is used in various applications, including as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential antioxidant properties and is sometimes used in the preparation of UV absorbers and stabilizers for polymers. The compound's ability to form complexes with metal ions makes it a candidate for use in analytical chemistry and as a chelating agent.

3487-81-8

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3487-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3487-81-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3487-81:
(6*3)+(5*4)+(4*8)+(3*7)+(2*8)+(1*1)=108
108 % 10 = 8
So 3487-81-8 is a valid CAS Registry Number.

3487-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxy-phenoxy)-benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-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:3487-81-8 SDS

3487-81-8Relevant academic research and scientific papers

Efficient Aryl Migration from an Aryl Ether to a Carboxylic Acid Group To Form an Ester by Visible-Light Photoredox Catalysis

Wang, Shao-Feng,Cao, Xiao-Ping,Li, Yang

, p. 13809 - 13813 (2017/10/24)

We have developed a highly efficient aryl migration from an aryl ether to a carboxylic acid group through retro-Smiles rearrangement by visible-light photoredox catalysis at ambient temperature. Transition metals and a stoichiometric oxidant and base are avoided in the transformation. Inspired by the high efficiency of this transformation and the fundamental importance of C?O bond cleavage, we developed a novel approach to the C?O cleavage of a biaryl ether to form two phenolic compounds, as demonstrated by a one-pot, two-step gram-scale reaction under mild conditions. The aryl migration exhibits broad scope and can be applied to the synthesis of pharmaceutical compounds, such as guacetisal. Primary mechanistic studies indicate that the catalytic cycle occurs by a reductive quenching pathway.

COMPOUNDS WITH 7-MEMBER CYCLE AND THE PHARMACEUTICAL USE THEREOF FOR PREVENTING AND TREATING DIABETES AND METABOLISM SYNDROME

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Page/Page column 31-32, (2010/07/06)

The invention discloses a new use of a class of heptacyclic compounds in the preparation of formulations for the prevention and treatment of diabetes and metabolic syndromes; the present invention also discloses a new class of heptacyclic compounds; the present invention also discloses a process for preparing the heptacyclic compounds and a composition containing the same. The heptacyclic compounds of the present invention can be used to effectively preventing or treating diseases such as diabetes and metabolic syndromes.

Leukotriene antagonists

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, (2008/06/13)

This invention provides tricyclic derivatives which are leukotriene B4 antagonists, formulations of those derivatives, and a method of using those derivatives for the treatment of conditions characterized by an excessive release of leukotrienes

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