Basic information Safety Supplier Related

methyl 3-hydroxy-5-nitro-benzoate

Basic information Safety Supplier Related

methyl 3-hydroxy-5-nitro-benzoate Basic information

Product Name:
methyl 3-hydroxy-5-nitro-benzoate
Synonyms:
  • methyl 3-hydroxy-5-nitro-benzoate
  • Benzoic acid, 3-hydroxy-5-nitro-, methyl ester
  • 3-hydroxy-5-nitrobenzoic acid, methyl ester
CAS:
55076-32-9
MF:
C8H7NO5
MW:
197.14
Mol File:
55076-32-9.mol
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methyl 3-hydroxy-5-nitro-benzoate Chemical Properties

Melting point:
154-156 °C
Boiling point:
377.2±27.0 °C(Predicted)
Density 
1.432±0.06 g/cm3(Predicted)
pka
7.52±0.10(Predicted)
form 
powder
color 
Light yellow
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Safety Information

HS Code 
2918290090
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methyl 3-hydroxy-5-nitro-benzoate Usage And Synthesis

Uses

Methyl 3-hydroxy-5-nitrobenzoate is a derivative of benzoic acid (B203900). Methyl 3-hydroxy-5-nitrobenzoate is used in synthetic preparations.

Synthesis

67-56-1

78238-14-9

55076-32-9

1. 3-Hydroxy-5-nitrobenzoic acid (3.7 g, 20.00 mmol) was dissolved in methanol (70.0 mL) at 0 °C. 2. Thionyl chloride (12.0 mL) was slowly added to the above solution. 3. The temperature of the reaction mixture was raised to 6 °C and stirred continuously for 3 hours. 4. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. 5. Water was added to the residue and subsequently extracted with ethyl acetate. 6. The organic phases were combined, washed with saturated brine and dried over anhydrous sodium sulfate. 7. After filtration, the organic phase was concentrated under reduced pressure to afford the crude product methyl 3-hydroxy-5-nitrobenzoate (3.9 g) as an off-white solid which did not require further purification. 8. The structure of the product was determined by 1H-1H-beta-hydroxy-5-nitrobenzoic acid. 8. The structure of the product was confirmed by 1H-NMR (300 MHz, DMSO-d6): δ 10.96 (s, 1H), 8.08 (m, 1H), 7.78 (m, 1H), 7.70 (m, 1H), 3.90 (s, 3H).

References

[1] Journal of Medicinal Chemistry, 2016, vol. 59, # 10, p. 4812 - 4830
[2] Patent: US2014/350007, 2014, A1. Location in patent: Paragraph 0076; 0077; 0078
[3] Journal of Medicinal Chemistry, 1984, vol. 27, # 12, p. 1549 - 1559
[4] Patent: US2010/69431, 2010, A1. Location in patent: Page/Page column 110-111
[5] Patent: WO2014/196793, 2014, A1. Location in patent: Page/Page column 74

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