2-Fluoro-6-methoxybenzylamine

2-Fluoro-6-methoxybenzylamine Suppliers list
Company Name: Zhijiang City Zhou Yuan Yao Biological Technology Co., LTD  Gold
Tel: 15671050515
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Company Name: J & K SCIENTIFIC LTD.  
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Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
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Company Name: Capot Chemical Co., Ltd  
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Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  
Tel: 15721252604 17321035817
Email: sales@harvest-chem.com

2-Fluoro-6-methoxybenzylamine manufacturers

2-Fluoro-6-methoxybenzylamine Basic information
Product Name:2-Fluoro-6-methoxybenzylamine
Synonyms:RARECHEM AL BW 0472;(2-Fluoro-6-methoxyphenyl)methylamine;2-Fluoro-6-methoxybenzenemethanamine;Benzenemethanamine, 2-fluoro-6-methoxy- (9CI);1-(2-fluoro-6-methoxyphenyl)methanamine;Benzenemethanamine, 2-fluoro-6-methoxy-;2-Fluoro-6-methoxybenzylamine
CAS:150517-75-2
MF:C8H10FNO
MW:155.17
EINECS:
Product Categories:HALIDE;Amine
Mol File:150517-75-2.mol
2-Fluoro-6-methoxybenzylamine Structure
2-Fluoro-6-methoxybenzylamine Chemical Properties
Boiling point 76-77°C/3.2mm
density 1.127±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka8.72±0.10(Predicted)
form liquid
color clear
InChIInChI=1S/C8H10FNO/c1-11-8-4-2-3-7(9)6(8)5-10/h2-4H,5,10H2,1H3
InChIKeyJCXMQSDLDAJYMF-UHFFFAOYSA-N
SMILESC1(CN)=C(OC)C=CC=C1F
Safety Information
HS Code 2922290090
MSDS Information
2-Fluoro-6-methoxybenzylamine Usage And Synthesis
Synthesis
2-Fluoro-6-methoxybenzonitrile

94088-46-7

2-FLUORO-6-METHOXYBENZYLAMINE

150517-75-2

General procedure for the synthesis of 2-fluoro-6-methoxybenzylamine from 2-fluoro-6-methoxybenzonitrile: 30 g of Raney nickel catalyst was added to a 1.0 L methanol solution containing 2-fluoro-6-methoxybenzonitrile (228 g, crude) and 145 mL ammonium hydroxide. The reaction mixture was transferred to an autoclave and stirred at 40 °C and 25 atm hydrogen atmosphere for 8 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to give a light yellow oil. The oily material was further purified by decompression distillation to give 2-fluoro-6-methoxybenzylamine (60 g, 54% yield) as a colorless oil. The product was characterized by 1H NMR (500 MHz, DMSO-d6): δ 1.58 (s, 2H), 3.67 (s, 1H), 6.75 (t, 1H), 6.82 (d, 1H), 7.22 (dd, 1H).LC-MS analysis showed [MH]+ = 156.1.

References[1] Patent: WO2017/221092, 2017, A1. Location in patent: Paragraph 00154
[2] Patent: WO2017/221100, 2017, A1. Location in patent: Paragraph 00149
2-Fluoro-6-methoxybenzylamine Preparation Products And Raw materials
Raw materials2-Fluoro-6-methoxybenzonitrile-->Ammonium hydroxide-->Hydrogen-->Methanol
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