5-Fluoro-2-methoxyaniline CAS 1978-39-8

Introduction:Basic information about 5-Fluoro-2-methoxyaniline CAS 1978-39-8, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

5-Fluoro-2-methoxyaniline Basic information

Product Name:5-Fluoro-2-methoxyaniline
Synonyms:5-Fluoro-o-anisidine (NH2=1);2-amino-4-fluoro-1-methoxybenzene;2-amino-4-fluoroanisole;5-fluoro-2-methoxybenzenamine;5-fluoro-o-anisidine;2-Amino-4-fluoroanisole5-Fluoro-o-anisidine2-Amino-4-fluoro-1-methoxybenzene;2-Amino-4-fluoroanisole, 5-Fluoro-o-anisidine;2-AMino-4-fluoroanisole[5-Fluoro-2-Methoxyaniline]
CAS:1978-39-8
MF:C7H8FNO
MW:141.14
EINECS:
Product Categories:Amines;blocks;FluoroCompounds;Aniline;Phenyls & Phenyl-Het
Mol File:1978-39-8.mol

5-Fluoro-2-methoxyaniline Chemical Properties

Melting point 3 °C
Boiling point 90 °C/760 mmHg
density 1.1981 g/mL at 25 °C
refractive index n20/D 1.5438
Fp 109 °C
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka3.52±0.10(Predicted)
form clear liquid
color Colorless to Light yellow to Light orange
InChI1S/C7H8FNO/c1-10-7-3-2-5(8)4-6(7)9/h2-4H,9H2,1H3
InChIKeyVYZUBHRSGQAROM-UHFFFAOYSA-N
SMILESCOc1ccc(F)cc1N
CAS DataBase Reference1978-39-8

Safety Information

Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 26
RIDADR UN 2810 6.1/PG III
WGK Germany 3
HazardClass 6.1
PackingGroup III
HS Code 2921420090
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

5-Fluoro-2-methoxyaniline Usage And Synthesis

Uses5-Fluoro-2-methoxyaniline was used in the study of structure-activity relationship to discover selective inhibitors of p97 ATPase.
Synthesis

445-83-0

1978-39-8

General procedure for the synthesis of 2-methoxy-5-fluoroaniline from 2-nitro-4-fluoroanisole: 4-fluoro-2-nitroanisole (85 g, 0.50 mol) was dissolved in methanol (300 mL) and palladium-carbon catalyst (10%, 8 g) was added. The reaction was stirred under hydrogen atmosphere for 15 hours. After completion of the reaction, the catalyst was removed by filtration, and the filtrate was concentrated to dryness to obtain the crude product 2-methoxy-5-fluoroaniline (61.5 g, 0.436 mol, 87% yield), which could be directly used in the next reaction without further purification.

References[1] Collection of Czechoslovak Chemical Communications, 1982, vol. 47, # 1, p. 72 - 87
[2] Patent: WO2005/26137, 2005, A2. Location in patent: Page/Page column 231
[3] Journal of Organic Chemistry, 1951, vol. 16, p. 1345,1348
[4] Journal of the American Chemical Society, 1959, vol. 81, p. 94,95, 97
[5] Journal of Organic Chemistry, 1952, vol. 17, p. 229,230

5-Fluoro-2-methoxyaniline Preparation Products And Raw materials

Raw materials4-Fluoro-2-nitroanisole-->Hydrogen-->Methanol
Preparation Products2-Bromo-4-fluoroanisole-->2-Chloro-4-fluorophenol-->5-Fluoro-8-methoxyquinoline
5-FLUORO-2-METHOXYACETOPHENONE CAS 445-82-9
5-Fluoro-2-nitroanisole CAS 448-19-1
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