Basic information Safety Supplier Related

METHYL 2-AMINO-5-METHYLBENZOATE

Basic information Safety Supplier Related

METHYL 2-AMINO-5-METHYLBENZOATE Basic information

Product Name:
METHYL 2-AMINO-5-METHYLBENZOATE
Synonyms:
  • METHYL 2-AMINO-5-METHYLBENZOATE
  • Methyl 5-methylanthranilate
  • [2-(Methoxycarbonyl)phenyl]aMine
  • NSC 3109
  • o-(Methoxycarbonyl)aniline
  • SunaroMe UVA
  • 5-Methyl-2-aMinobenzoic acid Methyl ester
  • 2-Amino-5-methylbenzoic acid methyl ester
CAS:
18595-16-9
MF:
C9H11NO2
MW:
165.19
Product Categories:
  • Aromatics Compounds
  • Aromatics
Mol File:
18595-16-9.mol
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METHYL 2-AMINO-5-METHYLBENZOATE Chemical Properties

Melting point:
54-56°C
Density 
1.132
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Dichloromethane, Ethyl Acetate, Methanol
form 
Solid
color 
Yellow to Brown
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Safety Information

HS Code 
2922498590
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METHYL 2-AMINO-5-METHYLBENZOATE Usage And Synthesis

Chemical Properties

METHYL 2-AMINO-5-METHYLBENZOATE is yellow Solid

Uses

METHYL 2-AMINO-5-METHYLBENZOATE is a useful synthetic intermediate

Uses

A useful synthetic intermediate.

Synthesis

20587-30-8

18595-16-9

Methyl 5-methyl-2-nitrobenzoate (8 g, 41.025 mmol) was used as a raw material in a solvent mixture of methanol (80 mL) and water (10 mL), and cooled to 0 °C. Subsequently, zinc powder (13.33 g, 205.128 mmol) and NH4Cl (17.6 g, 328.2 mmol) were added sequentially. The reaction mixture was stirred at room temperature for 12 h. The reaction progress was monitored by TLC (unfolding agent: 20% ethyl acetate/hexane). After completion of the reaction, the mixture was filtered and the filtrate was evaporated to give the crude product. The crude product was alkalized with saturated NaHCO3 solution and extracted with dichloromethane (2 x 20 mL). The organic layers were combined, dried with Na2SO4, filtered and the solvent was evaporated to give the target compound methyl 2-amino-5-methylbenzoate (yield: 4 g, 60%).1H NMR (400 MHz, CDCl3) data were as follows: δ 7.65 (s, 1H), 7.25 (s, 1H), 7.10-7.07 (q, 1H, J=8Hz), 6.58 (d, 1H), 3.86 (s, 3H), 2.22 (s, 3H).

References

[1] Patent: WO2015/38417, 2015, A1. Location in patent: Paragraph 151; 152
[2] Journal of the Chemical Society, 1930, p. 1513,1516
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 15, p. 4416 - 4420
[4] Patent: EP1475368, 2004, A1. Location in patent: Page 57

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