ChemicalBook > Product Catalog >Chemical Reagents >Organic reagents >Aromatic acids >2-Fluoro-6-nitrobenzoic acid

2-Fluoro-6-nitrobenzoic acid

2-Fluoro-6-nitrobenzoic acid Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Liaoning Tianhua Chemical Co., Ltd.  
Tel: 0418-6530555 2855550
Email:
Company Name: INTATRADE GmbH  
Tel: +49 3493/605464
Email: sales@intatrade.de
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com

2-Fluoro-6-nitrobenzoic acid manufacturers

2-Fluoro-6-nitrobenzoic acid Basic information
Product Name:2-Fluoro-6-nitrobenzoic acid
Synonyms:2-Carboxy-3-fluoronitrobenzene;Benzoicacid, 2-fluoro-6-nitro-;2-FLUORO-6-NITROBENZOIC ACID;2-FLUORO-6-NITROBENZOIC ACID 98.0%;2-Fluoro-6-nitrobenzotc acid;6-Fluoro-2-nitrobenzoic Acid;2-Flouride-6-Nitro Benzoic Acids;uoro-6-nitrobenzoic acid
CAS:385-02-4
MF:C7H4FNO4
MW:185.11
EINECS:253-994-5
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Acids and Derivatives;Benzoic acid;Benzoic acid series
Mol File:385-02-4.mol
2-Fluoro-6-nitrobenzoic acid Structure
2-Fluoro-6-nitrobenzoic acid Chemical Properties
Melting point 150 °C
Boiling point 334.7±27.0 °C(Predicted)
density 1.568±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka1.50±0.30(Predicted)
form Solid
color White to Light yellow to Light orange
CAS DataBase Reference385-02-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
HS Code 29163900
MSDS Information
2-Fluoro-6-nitrobenzoic acid Usage And Synthesis
Chemical Propertieslight yellow powder
Uses2-Fluoro-6-nitrobenzoic acid is used as an intermediate in the synthesis of certain drugs, pesticides or advanced materials.
Synthesis
2-Fluoro-6-nitrotoluene

769-10-8

2-Fluoro-6-nitrobenzoic acid

385-02-4

A. Synthesis of 2-fluoro-6-nitrobenzoic acid. Under stirring, 2-fluoro-6-nitrotoluene (exact amount not provided) was added to a suspension of potassium permanganate (102 g, 0.65 mol) in water (1.4 L). The reaction mixture was heated to reflux for 4 h, subsequently cooled to room temperature, filtered and washed with diethyl ether. The aqueous phase was acidified to pH 2 with concentrated hydrochloric acid and then extracted with ethyl acetate. The organic phase was washed with brine, dried over magnesium sulfate, filtered, and concentrated under vacuum to give 11.81 g (40% yield) of 2-fluoro-6-nitrobenzoic acid. The product was characterized by 1H NMR and IS-MS (m/e 184.0 [M-1]). Elemental analysis (C7H4FNO4) Calculated values: C, 45.42; H, 2.18; N, 7.57; Measured values: C, 45.22; H, 2.29; N, 7.27.

References[1] Chemische Berichte, 1896, vol. 29, p. 841
[2] Journal of Medicinal Chemistry, 1994, vol. 37, # 6, p. 758 - 768
[3] Israel Journal of Chemistry, 1964, vol. 2, p. 25 - 28
[4] Patent: US6635657, 2003, B1
[5] Patent: US4316839, 1982, A
Tag:2-Fluoro-6-nitrobenzoic acid(385-02-4) Related Product Information
1-Fluoro-2-nitrobenzene 3-Nitrobenzoic acid 4-Fluoronitrobenzene 4-Nitrobenzoic acid Methyl 4-fluoro-2-nitrobenzoate 4-FLUORO-3-NITROBENZOIC ACID ETHYL ESTER Fluorine 2,4-DICHLORO-5-FLUORO-3-NITROBENZOIC ACID 4-Fluoro-2-nitrobenzoic acid 2-Fluoro-5-nitrobenzoic acid Methyl 4-fluoro-3-nitrobenzoate 3-Fluoro-5-nitrobenzoic acid 4-Chloro-2-fluoro-5-nitrobenzoic acid tert-Butyl 2-fluoro-4-nitrobenzoate 2,3,4,5-Tetrafluoro-6-nitrobenzoic acid 2,4-Difluoro-5-nitrobenzoic acid 2-Amino-6-fluoro-3-nitrobenzoic acid ethyl ester 4,5-Difluoro-2-nitrobenzoic acid