207346-42-7

Basic information

• Product Name: Methyl 2-amino-4,5-difluorobenzoate
• Synonyms: Methyl 2-amino-4,5-difluorobenzoate;Benzoic acid, 2-amino-4,5-difluoro-, methyl ester (9CI);Benzoic acid, 2-amino-4,5-difluoro-, methyl ester;ETHYL2-AMINO-4,5-DIFLUOROBENZOATE;Methyl 2-amino-4,5-d;2-aMino-4,5-difluoro-benzoic acid,Methyl ester, Methyl 4,5-difluoroanthranilate, 2-aMino-4,5-difluoro-benzoic acid, Methyl ester, Methyl 2-aMino-4,5-difluorobenzoate
• CAS NO: 207346-42-7
• Molecular Formula: C₈H₇F₂NO₂
• Molecular Weight: 187.14
• Product Categories: AMINOACID;Phenylacetic acid;Esters;Phenyls & Phenyl-Het
• Mol File: 207346-42-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 274.1 °C at 760 mmHg
• Flash Point: 119.5 °C
• Appearance: White/Solid
• Density: 1.355 g/cm³
• Vapor Pressure: 0.00553mmHg at 25°C
• Refractive Index: 1.524
• Storage Temp.: Room temperature.
• PKA: 1.33±0.10(Predicted)
• CAS DataBase Reference: Methyl 2-amino-4,5-difluorobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-amino-4,5-difluorobenzoate(207346-42-7)
• EPA Substance Registry System: Methyl 2-amino-4,5-difluorobenzoate(207346-42-7)

Safety Data

• Hazardous Substances Data: 207346-42-7(Hazardous Substances Data)

Usage

General Description

Methyl 2-amino-4,5-difluorobenzoate is a chemical compound with the molecular formula C9H8F2NO2. It is an ester formed from methyl alcohol and 2-amino-4,5-difluorobenzoic acid. Methyl 2-amino-4,5-difluorobenzoate is a white crystalline solid that is used in the synthesis of pharmaceuticals and agrochemicals. It has two fluorine atoms attached to the benzene ring, which can make it useful in certain applications such as in the development of novel drugs. Additionally, the amino group on the benzene ring makes it a potential intermediate for the synthesis of other organic compounds. Methyl 2-amino-4,5-difluorobenzoate is a versatile compound with potential uses in various industries.

InChI:InChI=1/C8H7F2NO2/c1-13-8(12)4-2-5(9)6(10)3-7(4)11/h2-3H,11H2,1H3

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 83506-93-8 2-amino-4,5-difluorobenzoic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 1015433-96-1 methyl 4,5-difluoro-2-nitrobenzoate 
• 67-56-1 methanol 

Downstream Products

• 1255091-97-4 C₁₆H₁₀F₂N₂O₄ 
• 1015433-98-3 C₁₇H₁₄F₂N₂O₅ 
• 936500-97-9 C₉H₆ClF₂NO₃ 
• 207346-43-8 C₁₅H₁₀F₂N₂O₆ 
• 1079989-99-3 [4-(6-chloro-7-methylamino-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-phenyl]-5-chloro-thiophen-2-yl-sulfonylurea N-ethylglucamine salt 
• 1079989-95-9 [4-(6-chloro-7-methylamino-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-phenyl]-5-chloro-thiophen-2-yl-sulfonylurea L-lysine salt 
• 1079989-98-2 [4-(6-chloro-7-methylamino-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-phenyl]-5-chloro-thiophen-2-yl-sulfonylurea tromethamine salt 
• 936500-99-1 C₁₄H₉F₂N₃O₂*ClH 
• 936500-98-0 C₁₉H₁₇F₂N₃O₄ 

Relevant articles and documents

ANTIVIRAL COMPOUNDS

The present invention provides new antiviral compounds and pharmacological compositions comprising these new compounds and their use in the prophylaxis, prevention and treatment of viral infections, particularly adenovirus and herpes virus infections.

NEW ANTIVIRAL COMPOUNDS

The present invention provides new antiviral compounds and pharmacological compositions comprising these new compounds and their use in the prophylaxis, prevention and treatment of viral infections, particularly adenovirus and herpes virus infections.

4-Hydroxy-2-quinolones. 90.* Synthesis and antitubercular activity of 4-methyl-2-thiazolylamides of halo-substituted 4-hydroxy-2-oxo-1,2-dihydro-3- quinolinecarboxylic acids

Several variants were studied for the synthesis of esters of halogen derivatives of 4-hydroxy-2-oxo-1,2-dihydro-3-quinolinecarboxylic acids, whose reaction with 2-amino-4-methylthiazole gives the corresponding hetarylamides. Results are given for a study of the antitubercular activity of these products. 2006 Springer Science+Business Media, Inc.