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175277-86-8

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175277-86-8 Usage

General Description

3-Fluoro-4-methylbenzamide is a chemical compound with the molecular formula C8H8FNO. It is an aromatic amide with a fluorine atom at the 3-position and a methyl group at the 4-position on the benzene ring. 3-FLUORO-4-METHYLBENZAMIDE is commonly used as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. It is also used as a reagent in the synthesis of other organic compounds. 3-Fluoro-4-methylbenzamide is a white solid at room temperature and is soluble in organic solvents such as ethanol and acetone. It is important for its role as an intermediate in the production of numerous compounds in the pharmaceutical and chemical industries.

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 articles and documents

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, 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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