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3-Fluoro-4-methylbenzamide, an aromatic amide with the molecular formula C8H8FNO, is characterized by the presence of a fluorine atom at the 3-position and a methyl group at the 4-position on the benzene ring. This white solid at room temperature is soluble in organic solvents such as ethanol and acetone. It is a versatile building block in organic synthesis and serves as an intermediate in the production of various pharmaceuticals and agrochemicals.

175277-86-8

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175277-86-8 Usage

Uses

Used in Pharmaceutical Industry:
3-Fluoro-4-methylbenzamide is used as a key building block for the synthesis of a variety of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Fluoro-4-methylbenzamide is utilized as a precursor in the production of various agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used as a Reagent in Organic Synthesis:
3-Fluoro-4-methylbenzamide also serves as a reagent in the synthesis of other organic compounds, facilitating the creation of a wide range of chemical entities for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 175277-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,7 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175277-86:
(8*1)+(7*7)+(6*5)+(5*2)+(4*7)+(3*7)+(2*8)+(1*6)=168
168 % 10 = 8
So 175277-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8FNO/c1-5-2-3-6(8(10)11)4-7(5)9/h2-4H,1H3,(H2,10,11)

175277-86-8SDS

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 3-Fluoro-4-methylbenzamide

1.2 Other means of identification

Product number -
Other names 4-Carbamoyl-2-fluorotoluene

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:175277-86-8 SDS

175277-86-8Relevant academic research and scientific papers

In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis

Deb, Pran Kishore,Al-Shar’i, Nizar A.,Venugopala, Katharigatta N.,Pillay, Melendhran,Borah, Pobitra

, p. 869 - 884 (2021/06/11)

The alarming increase in multi- and extensively drug-resistant (MDR and XDR) strains of Mycobacterium tuberculosis (MTB) has triggered the scientific community to search for novel, effective, and safer therapeutics. To this end, a series of 3,5-disubstitu

Design, microwave assisted synthesis and characterization of substituted 1,2,4-oxadiazole analogues as promising pharmacological agents

Venugopala, Katharigatta N.

, p. 1767 - 1770 (2017/06/27)

Microwave assisted synthesis of a series of 3,5-disubstituted-1,2,4-oxadiazole analogues (3a-j) has been achieved between 5-(chloromethyl)-3-substituted phenyl-1,2,4-oxadiazoles (2a-j) and substituted benzophenone in presence of potassium carbonate in ace

Design, synthesis, characterization, and antibacterial activity of {5-chloro-2-[(3-substitutedphenyl-1,2,4-oxadiazol-5-yl)-methoxy]-phenyl} -(phenyl)-methanones

Rai, Neithnadka Premsai,Narayanaswamy, Venugopala Katharigatta,Govender, Thavendran,Manuprasad,Shashikanth, Sheena,Arunachalam, Pirama Nayagam

experimental part, p. 2677 - 2682 (2010/07/09)

In the present investigation, a series of novel {5-chloro-2-[(3-(substitutedphenyl)-1,2,4-oxadiazol-5-yl)-methoxy]-pheny l}-(phenyl)-methanones (3a-i) have been synthesized from 5-(chloromethyl)-3-substitutedphenyl-1,2,4-oxadiazole (2a-i). The newly synth

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