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3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID is a chemical compound characterized by the molecular formula C8H8FNO2. It is a fluorinated aromatic carboxylic acid featuring a methyl and an amino group attached to the benzene ring. 3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID is recognized for its versatile reactivity and potential biological activity, making it a valuable building block in the synthesis of various biologically active molecules and compounds.

103877-75-4

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103877-75-4 Usage

Uses

Used in Pharmaceutical Industry:
3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of biologically active molecules. Its unique molecular structure allows for the creation of compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID serves as an intermediate in the production of agrochemicals, leveraging its chemical properties to enhance the effectiveness of products designed for agricultural use.
Used in Organic Synthesis:
3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID is utilized in organic synthesis as a key component due to its reactive nature, facilitating the formation of a wide range of organic compounds for various applications.
Used in Medicinal Chemistry:
Within medicinal chemistry, 3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID is employed for its potential to be incorporated into the structures of new pharmaceutical agents, contributing to the discovery and development of innovative medications.

Check Digit Verification of cas no

The CAS Registry Mumber 103877-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,7 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103877-75:
(8*1)+(7*0)+(6*3)+(5*8)+(4*7)+(3*7)+(2*7)+(1*5)=134
134 % 10 = 4
So 103877-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H8FNO2/c1-4-6(9)2-5(8(11)12)3-7(4)10/h2-3H,10H2,1H3,(H,11,12)

103877-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-AMINO-5-FLUORO-4-METHYLBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 3-fluoro-4-methyl-5-amino-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:103877-75-4 SDS

103877-75-4Downstream Products

103877-75-4Relevant academic research and scientific papers

Mutasynthesis of fluorinated pactamycin analogues and their antimalarial activity

Almabruk, Khaled H.,Lu, Wanli,Li, Yuexin,Abugreen, Mostafa,Kelly, Jane X.,Mahmud, Taifo

supporting information, p. 1678 - 1681 (2013/07/05)

A mutasynthetic strategy has been used to generate fluorinated TM-025 and TM-026, two biosynthetically engineered pactamycin analogues produced by Streptomyces pactum ATCC 27456. The fluorinated compounds maintain excellent activity and selectivity toward chloroquine-sensitive and multidrug-resistant strains of malarial parasites as the parent compounds. The results also provide insights into the biosynthesis of 3-aminobenzoic acid in S. pactum.

Antibacterially active alkyl-1-cyclopropyl-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids

-

, (2008/06/13)

Alkyl-1-cyclopropyl-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids of the formula STR1 in which X1, X2 and X3 each independently is hydrogen, a nitro group, a halogen atom or an alkyl radical with 1 to 3 carbon atoms, with the proviso that at least one of them is an alkyl radical, or pharmaceutically acceptable salts or hydrates thereof, are antibacterially active and promote animal growth.

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