16633-50-4

Basic information

• Product Name: 2,6-DIMETHYL-4-FLUOROBENZOIC ACID
• Synonyms: RARECHEM AL BO 1056;2,6-DIMETHYL-4-FLUOROBENZOIC ACID;4-FLUORO-2,6-DIMETHYLBENZOIC ACID;2-Carboxy-5-fluoro-m-xylene;2,6-Dimethyl-4-fluorobenzoicacid97%
• CAS NO: 16633-50-4
• Molecular Formula: C₉H₉FO₂
• Molecular Weight: 168.16
• Product Categories: Carboxylic Acids;Phenyls & Phenyl-Het;Benzoic acid;Carboxylic Acids;Phenyls & Phenyl-Het
• Mol File: 16633-50-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 278.36 °C at 760 mmHg
• Flash Point: 122.148 °C
• Appearance: /
• Density: 1.212
• Vapor Pressure: 0.002mmHg at 25°C
• Refractive Index: 1.53
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.53±0.37(Predicted)
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2,6-DIMETHYL-4-FLUOROBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIMETHYL-4-FLUOROBENZOIC ACID(16633-50-4)
• EPA Substance Registry System: 2,6-DIMETHYL-4-FLUOROBENZOIC ACID(16633-50-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 16633-50-4(Hazardous Substances Data)

Usage

General Description

2,6-Dimethyl-4-fluorobenzoic acid is a chemical compound that falls under the category of aromatic organic compounds known as benzene and substituted derivatives. These compounds are characterized by a six-membered ring structure composed of five carbon atoms and one hydrocarbon. This specific type of benzoic acid is comprised of carboxylic acid with a fluorine atom respectively placed on the fourth carbon atom and two methyl groups at positions two and six. Due to its essential acid functionalities, it typically exhibits strong acidic behavior. Its applications can range from use in the production of dyes and other chemicals, to serve as intermediates in chemical reactions within various industries like pharmaceuticals, manufacturing, or even research. It may also hold potential for broader applications within fluorescence-based biological research and other specialized scientific fields.

InChI:InChI=1/C9H9FO2/c1-5-3-7(10)4-6(2)8(5)9(11)12/h3-4H,1-2H3,(H,11,12)

Upstream product

• 16643-19-9 4-Fluoro-2,6-dimethylbenzamide 
• 3095-38-3 3,5-dimethyl-4-nitrobenzoic acid 
• 315-12-8 2,6-dimethyl-4-fluoro-1-nitro-benzene 
• 34761-82-5 3,5-dimethyl-4-nitroaniline 
• 14659-61-1 2,6-dimethyl-4-fluorobenzonitrile 
• 19023-45-1 3,5-dimethyl-4-nitro-benzoic acid amide 
• 392-70-1 2,6-dimethyl-4-fluoroaniline 
• 14659-60-0 methyl 4‐fluoro‐2,6‐dimethylbenzoate 
• 124-38-9 carbon dioxide 
• 14659-58-6 2‐bromo‐5‐fluoro‐1,3‐dimethylbenzene 
• 110-05-4 di-tert-butyl peroxide 
• 321-21-1 4-fluoro-2-methylbenzoic acid 
• 456-22-4 4-Fluorobenzoic acid 

Downstream Products

• 14659-60-0 methyl 4‐fluoro‐2,6‐dimethylbenzoate 
• 1609401-44-6 4-fluoro-2,6-dimethyl-N-(quinolin-8-yl)benzamide 
• 896120-69-7 4-fluoro-2,6-dimethylbenzoyl chloride 

Relevant articles and documents

Milled Dry Ice as a C1 Source for the Carboxylation of Aryl Halides

The use of carbon dioxide as a C1 chemical feedstock remains an active field of research. Here we showcase the use of milled dry ice as a method to promote the availability of CO 2in a reaction solution, permitting practical synthesis of arylcarboxylic acids. Notably, the use of milled dry ice produces marked increases in yields relative to those obtained with gaseous CO 2, as previously reported in the literature.

Preparation method for o-tolylacetic acid aryl formic acid derivative

The invention discloses a preparation method for an o-tolylacetic acid aryl formic acid derivative. According to the method, new C-C bonds can be formed, the organic o-tolylacetic acid aryl formic acid derivative is obtained, the good functional group tolerance is achieved, and the o-tolylacetic acid aryl formic acid derivative which cannot be easily obtained by adopting other methods can be synthesized; according to the method, adopted raw materials are easy to obtain, the yield is high, the reaction conditions are mild, the substrate range is wide, and after-treatment is simple and green.

INHIBITORS OF STEAROYL-COA DESATURASE

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