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Methyl (2-amino-phenyl)-acetate

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Methyl (2-amino-phenyl)-acetate manufacturers

Methyl (2-amino-phenyl)-acetate Basic information
Product Name:Methyl (2-amino-phenyl)-acetate
Synonyms:Benzeneacetic acid, 2-aMino-, Methyl ester;Methyl 2-(2-aminophenyl);1H-Pyrrole-2,5-dione,5-methyl-;METHYL 2-(2-AMINOPHENYL)ACETATE;Methyl (2-amino-phenyl)-acetate
CAS:35613-44-6
MF:C9H11NO2
MW:165.19
EINECS:
Product Categories:
Mol File:35613-44-6.mol
Methyl (2-amino-phenyl)-acetate Structure
Methyl (2-amino-phenyl)-acetate Chemical Properties
Boiling point 277.5±15.0 °C(Predicted)
density 1.143±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka3.39±0.10(Predicted)
InChIInChI=1S/C9H11NO2/c1-12-9(11)6-7-4-2-3-5-8(7)10/h2-5H,6,10H2,1H3
InChIKeyBWQBYHGDMBHIIQ-UHFFFAOYSA-N
SMILESC1(CC(OC)=O)=CC=CC=C1N
Safety Information
HS Code 2922498590
MSDS Information
Methyl (2-amino-phenyl)-acetate Usage And Synthesis
UsesMethyl 2-(2-aminophenyl)acetate is used as an intermediate in organic synthesis.
Biological ActivityMethyl (2-amino-phenyl)-acetate has shown to have antiviral and antitumor properties, as well as potential use in cancer therapy.
Synthesis
METHYL (2-NITRO-PHENYL)-ACETATE

30095-98-8

METHYL (2-AMINO-PHENYL)-ACETATE

35613-44-6

General procedure for the synthesis of methyl (2-aminophenyl)acetate from methyl (2-nitrophenyl)acetate: [00231] A mixture of compounds 1-2 ((2-nitrophenyl)acetic acid methyl ester, 9.75 g, 50 mmol), 10% palladium carbon catalyst (dry, 530 mg, 5 mmol) in methanol (100 mL) was subjected to a hydrogen atmosphere and stirred at room temperature overnight. Upon completion of the reaction, the reaction mixture was filtered to remove the palladium-carbon catalyst, and the filtrate was concentrated to afford compound 6-1 ((2-aminophenyl)acetic acid methyl ester, 8.02 g, yield: 97%) as a light yellow oil. MS (ES): m/z: 166 [M + H]. 1H NMR (400MHz, DMSO-d6) δ: 6.94 (m, 2H), 6.64 (d, 1H, J=8.0Hz), 6.51 (m, 1H), 4.88 (s, 2H), 3.59 (s, 3H), 3.52 (s, 2H).

References[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 5, p. 691 - 701
[2] European Journal of Organic Chemistry, 2017, vol. 2017, # 14, p. 1889 - 1893
[3] Patent: WO2014/106238, 2014, A1. Location in patent: Paragraph 00231
[4] Patent: WO2014/106238, 2014, A1. Location in patent: Paragraph 00269; 00397
[5] Patent: WO2009/3970, 2009, A1. Location in patent: Page/Page column 42-43
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