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2-(3-chlorophenoxy)benzoic acid is an organic compound with the chemical formula C13H9ClO3. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 248.66 g/mol. 2-(3-chlorophenoxy)benzoic acid is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Its chemical structure features a benzoic acid core with a 3-chlorophenoxy group attached at the 2-position, which contributes to its reactivity and utility in chemical synthesis.

6312-85-2

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6312-85-2 Usage

Physical State

White crystalline solid

Chemical Structure

Combines a benzene ring with a carboxylic acid group and a 3-chlorophenol group

Usage

Synthetic herbicide used to control broadleaf weeds in crops like soybeans, peanuts, and rice

Mode of Action

Disrupts the growth of targeted weeds, leading to their death

Health Hazards

Potential skin and eye irritation; requires proper protective equipment for handling

Check Digit Verification of cas no

The CAS Registry Mumber 6312-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6312-85:
(6*6)+(5*3)+(4*1)+(3*2)+(2*8)+(1*5)=82
82 % 10 = 2
So 6312-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H9ClO3/c14-9-4-3-5-10(8-9)17-12-7-2-1-6-11(12)13(15)16/h1-8H,(H,15,16)

6312-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-chlorophenoxy)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:6312-85-2 SDS

6312-85-2Relevant academic research and scientific papers

A photoredox-neutral Smiles rearrangement of 2-aryloxybenzoic acids

Gonzalez-Gomez, Jose C.,Ramirez, Nieves P.,Lana-Villarreal, Teresa,Bonete, Pedro

supporting information, p. 9680 - 9684 (2017/11/30)

We report on the use of visible light photoredox catalysis for the radical Smiles rearrangement of 2-aryloxybenzoic acids to obtain aryl salicylates. The method is free of noble metals and operationally simple and the reaction can be run under mild batch or flow conditions. Being a redox neutral process, no stoichiometric oxidants or reductants are needed.

Carboxyl radical-assisted 1,5-aryl migration through Smiles rearrangement

Hossian, Asik,Jana, Ranjan

, p. 9768 - 9779 (2016/10/31)

We report herein, a silver(i)-catalyzed Smiles rearrangement of 2-aryloxy- or 2-(arylthio)benzoic acids to provide aryl-2-hydroxybenzoate or aryl-2-mercaptobenzoate dimer, respectively, through 1,5-aryl migration from oxygen or sulfur to carboxylate oxygen. Mechanistically, the aryl ether moiety undergoes an intramolecular ipso attack by the carboxyl radical followed by a C-O or C-S bond cleavage. Aryl-2-mercaptobenzoates undergo oxidative dimerization through a thiol moiety in situ.

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