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3-Fluoro-4-aminobenzonitrile

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Products Intro: Product Name:3-Fluoro-4-aminobenzonitrile
CAS:63069-50-1
Purity:99% Package:1KG;0.00;USD|25KG;0.00;USD
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Products Intro: Product Name:4-Amino-3-fluorobenzonitrile
CAS:63069-50-1
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CAS:63069-50-1
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Products Intro: Product Name:2-Fluoro-4-cyanoaniline
CAS:63069-50-1
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Products Intro: Product Name:3-Fluoro-4-aminobenzonitrile
CAS:63069-50-1
Purity:98% Package:1kg,5kg,10kg Remarks:pharmaceutical intermediates

3-Fluoro-4-aminobenzonitrile manufacturers

3-Fluoro-4-aminobenzonitrile Basic information
Product Name:3-Fluoro-4-aminobenzonitrile
Synonyms:4-AMINO-3-FLUOROBENZONITRILE;4-CYANO-2-FLUOROANILINE;3-FLUORO-4-AMINOBENZONITRILE;BUTTPARK 144\07-21;4-Amino-3-fluorobenzonitrile 98%;4-Amino-3-fluorobenzonitrile98%;4-Amino-3-Fluorobenzonitrile 3-Fluoro-4-Aminobenzonitrile;3-Fluoro-4-aminobenz
CAS:63069-50-1
MF:C7H5FN2
MW:136.13
EINECS:
Product Categories:Amines;blocks;Carboxes;FluoroCompounds;Aromatic Nitriles;Fluorobenzonitrile Series
Mol File:63069-50-1.mol
3-Fluoro-4-aminobenzonitrile Structure
3-Fluoro-4-aminobenzonitrile Chemical Properties
Melting point 70-74
Boiling point 264.2±25.0 °C(Predicted)
density 1.25±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka0.33±0.10(Predicted)
color White to Light yellow to Light orange
InChIKeyRLMBRRQWBTWGMB-UHFFFAOYSA-N
CAS DataBase Reference63069-50-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T
Risk Statements 20/21/22-36/38
Safety Statements 26-36/37
RIDADR UN3439
Hazard Note Irritant
HazardClass 6.1
PackingGroup III
HS Code 29269090
MSDS Information
3-Fluoro-4-aminobenzonitrile Usage And Synthesis
Chemical PropertiesOff-white to brown crystalline
Uses4-Amino-3-fluorobenzonitrile is used in preparation of substituted 1,6-Naphthyridine inhibitors of CDK5.
Synthesis
2-Fluoro-4-iodoaniline

29632-74-4

Copper(I) Cyanide

544-92-3

3-Fluoro-4-aminobenzonitrile

63069-50-1

Step 1: Synthesis of 4-amino-3-fluorobenzonitrile 2-Fluoro-4-iodoaniline (2.0 g, 8.4 mmol) and cuprous cyanide (982 mg, 11.0 mmol, 1.5 eq.) were added to N,N-dimethylformamide (DMF, 30 mL). The reaction mixture was heated to 130 °C and the reaction was stirred at this temperature for 8 hours. After completion of the reaction, the mixture was cooled to room temperature and diluted with ethyl acetate. The diluted solution was washed sequentially with deionized water (2 times) and saturated saline, and then dried with anhydrous magnesium sulfate. The dried solution was concentrated by filtration and the crude product obtained was purified by column chromatography (eluent: n-hexane/ethyl acetate = 3:1, v/v) to give the white solid product 4-amino-3-fluorobenzonitrile (914 mg, 84% yield). 1H NMR (300 MHz, CDCl3): δ 7.21-7.26 (m, 2H), 6.74 (t, 1H, J = 8.3 Hz), 4.20 (bs, 2H).

References[1] Patent: WO2007/120012, 2007, A1. Location in patent: Page/Page column 82-83; 129
[2] Patent: WO2006/63113, 2006, A2. Location in patent: Page/Page column 68-69
3-Fluoro-4-aminobenzonitrile Preparation Products And Raw materials
Raw materials2-Fluoro-4-iodoaniline-->3-Fluoro-4-nitrobenzonitrile-->Copper(I) Cyanide
Preparation Products4-acetyl-3-fluorobenzonitrile
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