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Methyl 3-chloro-5-fluorobenzoate is a chemical compound with the molecular formula C8H6ClFO2. It is a derivative of benzoic acid, featuring a methyl group, a chlorine atom, and a fluorine atom attached to a benzene ring. methyl 3-chloro-5-fluorobenzoate is recognized for its utility in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique properties make it a valuable building block for constructing more complex molecules, and it is widely used as an intermediate in the manufacturing of various chemical products. Due to its potential hazards if not handled properly, safety precautions are essential when working with methyl 3-chloro-5-fluorobenzoate.

327056-75-7

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327056-75-7 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3-chloro-5-fluorobenzoate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with targeted actions against diseases.
Used in Agrochemical Industry:
In the agrochemical sector, methyl 3-chloro-5-fluorobenzoate is utilized as a precursor in the production of pesticides and other crop protection agents. Its chemical structure provides a foundation for the design of effective compounds that can protect crops from pests and diseases.
Used in Organic Synthesis:
Methyl 3-chloro-5-fluorobenzoate serves as a versatile building block in organic synthesis, enabling the creation of a wide range of complex organic molecules for various applications. Its presence in the molecular structure can influence the reactivity and selectivity of synthetic reactions, leading to the production of desired compounds in research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 327056-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,0,5 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 327056-75:
(8*3)+(7*2)+(6*7)+(5*0)+(4*5)+(3*6)+(2*7)+(1*5)=137
137 % 10 = 7
So 327056-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClFO2/c1-12-8(11)5-2-6(9)4-7(10)3-5/h2-4H,1H3

327056-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-chloro-5-fluorobenzoate

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:327056-75-7 SDS

327056-75-7Relevant academic research and scientific papers

Piperidine compound and preparation method and medical application thereof

-

Paragraph 0384-0395; 0400; 0414-0419, (2021/04/07)

The invention discloses a piperidine compound shown as a formula (I) and a preparation method and medical application thereof, and particularly relates to a piperidine USP7 inhibitor compound or pharmaceutically acceptable salt or ester or solvate thereof and a preparation method and application of the piperidine USP7 inhibitor compound or pharmaceutically acceptable salt or ester or solvate thereof. The compound provided by the invention can inhibit the activity of USP7 enzyme, has very good selectivity and druggability, and can be used for preparing medicines for preventing or treating tumor diseases or virus infectious diseases.

Copper-Mediated Fluorination of Aryl Trisiloxanes with Nucleophilic Fluoride

Dorel, Ruth,Boehm, Philip,Schwinger, Daniel P.,Hartwig, John F.

supporting information, p. 1759 - 1762 (2020/02/05)

A method for the nucleophilic fluorination of heptamethyl aryl trisiloxanes to form fluoroarenes is reported. The reaction proceeds in the presence of Cu(OTf)2 and KHF2 as the fluoride source under mild conditions for a broad range of heptamethyltrisiloxyarenes with high functional group tolerance. The combination of this method with the silylation of aryl C?H bonds enables the regioselective fluorination of non-activated arenes controlled by steric effects following a two-step protocol.

Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists

-

, (2008/06/13)

The present invention provides compounds and pharmaceutical compositions that act as antagonists at metabotropic glutamate receptors, and that are useful for treating neurological diseases and disorders. Methods of preparing the compounds also are disclosed.

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