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5-Fluoro-2-methoxybenzoic acid is an organic compound that features a fluorine atom at the 5-position, a methoxy group at the 2-position, and a carboxylic acid functional group. It is a white crystalline solid and is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals.

394-04-7

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394-04-7 Usage

Uses

Used in Pharmaceutical Industry:
5-Fluoro-2-methoxybenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals, including antibiotics, anti-inflammatory drugs, and anticancer agents. Its unique structure allows for the development of new drugs with improved potency and selectivity.
Used in Agrochemical Industry:
5-Fluoro-2-methoxybenzoic acid is also used as an intermediate in the synthesis of agrochemicals, such as herbicides and insecticides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, leading to increased crop yields and reduced environmental impact.
Used in Organic Synthesis:
5-Fluoro-2-methoxybenzoic acid serves as a versatile building block in organic synthesis, allowing for the preparation of a wide range of organic compounds with diverse applications. Its reactivity and functional group compatibility make it a valuable component in the synthesis of specialty chemicals, dyes, and other materials.
Used in Research and Development:
5-Fluoro-2-methoxybenzoic acid is utilized in research and development settings to explore new chemical reactions and synthetic pathways. Its unique properties and reactivity make it an attractive candidate for studying novel chemical transformations and developing new synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 394-04-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 394-04:
(5*3)+(4*9)+(3*4)+(2*0)+(1*4)=67
67 % 10 = 7
So 394-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7FO3/c1-12-7-3-2-5(9)4-6(7)8(10)11/h2-4H,1H3,(H,10,11)

394-04-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H32389)  5-Fluoro-2-methoxybenzoic acid, 97%   

  • 394-04-7

  • 1g

  • 931.0CNY

  • Detail
  • Alfa Aesar

  • (H32389)  5-Fluoro-2-methoxybenzoic acid, 97%   

  • 394-04-7

  • 5g

  • 3871.0CNY

  • Detail
  • Aldrich

  • (523097)  5-Fluoro-2-methoxybenzoicacid  97%

  • 394-04-7

  • 523097-5G

  • 1,138.41CNY

  • Detail

394-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 5-FLUORO-2-METHOXYBENZOIC 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:394-04-7 SDS

394-04-7Relevant academic research and scientific papers

INHIBITORS OF THE MENIN-MLL INTERACTION

-

, (2018/01/17)

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

Leukotriene A4 hydrolase and cyclooxygense double target inhibitors and use thereof

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, (2016/10/07)

The invention discloses a double-target inhibitor for leukotriene A4 hydrolase and cyclooxygenase as well as a purpose of the double-target inhibitor. The double-target inhibitor is a compound shown in a general formula (I), wherein X1 and X2 are respectively and independently separated into hydrogen, halogen, alkyl or alkoxy; Y represents hydrogen, hydroxyl, halogen or alkyl; Z represents substituent groups at the fourth position and/or the fifth position of a benzoyl core benzene ring, and respectively represents hydrogen, halogen, amino, alkyl acylamino, alkyl substituted amino, trifluoromethyl or carboxyl alkyl acylamino; n is 2 to 4. The compound can be used for preparing medicine for treating, preventing or inhibiting inflammation such as arthritis and rheumatoid arthritis.

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