3-Fluoro-2-methoxyaniline
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3-Fluoro-2-methoxyaniline
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CAS No:
437-83-2
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Formula:
C7H8FNO
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Chemical Name:
3-Fluoro-2-methoxyaniline
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Synonyms:
3-fluoro-O-anisidine;3-Fluoro-2-methoxyan;3-Fluoro-2-Methoxyailine;3-Fuloro-2-methoxyaniline;3-FLUORO-2-METHOXYANILINE;3-FLUORO-2-METHOXYBENZENAMINE;3-Fluoro-2-methoxyaniline99%;3-Fluoro-2-methoxyaniline,JRD;3-FLUORO-2-METHOXY-PHENYLAMINE;3-Fluoro-2-methoxybenzenenamine
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CAS No:
Characteristics
35.2
1.3
Brown crystal
1.2±0.1 g/cm3
162 °C
217.9°C at 760 mmHg
42.2±0.0 °C
1.532
0.129mmHg at 25°C
Safety Information
III
3.2
UN 1993 3/PG 1
3
R11
16-26-36
F: Flammable;Xi: Irritant;
P261-P280-P301 + P310-P305 + P351 + P338-P312
H301-H311-H315-H319-H335
|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
3-Fluoro-2-methoxyaniline Use and Manufacturing
General procedure: The starting materials 1 and 2 were commercially available (Energy Chemical, Shanghai, China).Compound 2 (3.72 mmol) was added to a stirred solution of compound 1 (3.38 mmol) in glacial aceticacid (10 mL). The reaction mixture was then stirred at 110 C for 4 h. After completion of the reaction, the solvent was evaporated, and the residue was purified on a silica gel column chromatography andeluted with ethyl acetate/petroleum ether (bp 60-90 C) (1:3, v/v) to give compounds 3.
Computed Properties
Molecular Weight:141.14
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:141.058992041
Monoisotopic Mass:141.058992041
Topological Polar Surface Area:35.2
Heavy Atom Count:10
Complexity:110
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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