2-Amino-5-fluorobenzoic acid CAS No.446-08-2

Names and Identifiers Name 2-Amino-5-fluorobenzoic acid Synonyms NSC 513308 AURORA KA-5382 RARECHEM AL BO 2236 2-Amino-5-fluorobenzoic 5-FLUOROANTHRANILIC ACID 2-amino-5-fluorobenzoate Anthran...

Introduction

Names and Identifiers

Name 2-Amino-5-fluorobenzoic acid
Synonyms NSC 513308
AURORA KA-5382
RARECHEM AL BO 2236
2-Amino-5-fluorobenzoic
5-FLUOROANTHRANILIC ACID
2-amino-5-fluorobenzoate
Anthranilic acid, 5-fluoro-
2-AMINO-5-FLUOROBENZOIC ACID
2-aMino-5-fluorobenzoic aicd
2-Amino-5-fluorobenzoic acid
2-Amino-5-fluoroBenzoicacid97.
2-Amino-5-fluorobenzoic Acid, 5-FAA
5-Fluoroanthranilic acid, 2-Carboxy-4-fluoroaniline
2-Amino-5-fluorobenzoic acid (5-Fluoroanthranilic acid)
CAS 446-08-2
EINECS 207-159-7
InChI InChI=1/C7H6FNO2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,9H2,(H,10,11)/p-1
InChIKey FPQMGQZTBWIHDN-UHFFFAOYSA-N

​Physico-chemical Properties

Molecular Formula C7H6FNO2
Molar Mass 155.13
Density 1.3021 (estimate)
Melting Point 181-183°C(lit.)
Boling Point 223.67°C (rough estimate)
Flash Point 146.2°C
Solubility DMSO (Slightly), Methanol (Slightly)
Vapor Presure 0.000154mmHg at 25°C
Appearance White to bright yellow powder
Color Light yellow to light brown
BRN 2803664
pKa 1.86±0.10(Predicted)
Storage Condition Keep in dark place,Inert atmosphere,Room temperature
MDL MFCD00055566
Physical and Chemical Properties Appearance: light yellow crystal Melting Point: 181-183 ℃

Risk and Safety

Risk Codes 36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 – Wear suitable protective clothing.
S37/39 – Wear suitable gloves and eye/face protection
WGK Germany 3
HS Code 29224999
Hazard Class IRRITANT

Reference Information

use 2-amino -5-fluorobenzoic acid is a very important precursor for synthetic drugs, herbicides, plant growth regulators and quinoline fungicides.
medical use 2-amino-5-fluorobenzoic acid can be used as a precursor of the virucidal agent of HIV infectious diseases; as a precursor of the antiviral agent of herpes virus; Preparation of alcinine and its analogs as hypoglycemic reagents for the treatment of diabetes; preparation of aminoquinoline as an anti-cancer reagent; preparation of triazoquinolinones and their analogs for neuroprotective agents in ischemia, hypoglycemia, cerebral vasospasm, Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, atrophy, myelopathy and schizophrenia.
Synthesis method Synthesis of 5-fluoro-anthranilic acid using 2-methyl-4-fluoro-nitrobenzene as the starting material. It uses Raney nickel as a catalyst, and undergoes catalytic hydrogenation reduction with 2-methyl-4-fluoronitrobenzene at 50°C. After the catalyst is filtered, the solvent is removed by distillation to obtain 5-fluoro-2-Aminotoluene is oxidized with potassium permanganate, and the crude product is filtered after acidification, and purified by alkali dissolution and acid analysis to obtain a purer final target product.

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