Basic information Safety Supplier Related

Methyl 5-formyl-2-hydroxybenzoate

Basic information Safety Supplier Related

Methyl 5-formyl-2-hydroxybenzoate Basic information

Product Name:
Methyl 5-formyl-2-hydroxybenzoate
Synonyms:
  • 5-FORMYL-2-HYDROXYBENZOIC ACID METHYL ESTER
  • Methyl 5-formyl-2-hydroxybenzoate
  • 5-formylsalicylic acid methyl ester
  • 2-Hydroxy-5-formylbenzoic acid methyl ester
  • Methyl 5-Formylsalicylate
  • 5-Formylsalicylic Acid Methyl Ester Methyl 5-Formyl-2-hydroxybenzoate 5-Formyl-2-hydroxybenzoic Acid Methyl Ester
  • Isophthalaldehydic acid, 6-hydroxy-, methyl ester
  • Methyl 5-formyl-2-hydroxybenzoate in stock Factory
CAS:
41489-76-3
MF:
C9H8O4
MW:
180.16
EINECS:
677-591-2
Product Categories:
  • API intermediates
  • Acids and Derivatives
  • Carbonyl Compounds
Mol File:
41489-76-3.mol
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Methyl 5-formyl-2-hydroxybenzoate Chemical Properties

Melting point:
79.0 to 83.0 °C
Boiling point:
294.5±25.0 °C(Predicted)
Density 
1.310±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
7.57±0.18(Predicted)
color 
White to Light yellow
InChI
InChI=1S/C9H8O4/c1-13-9(12)7-4-6(5-10)2-3-8(7)11/h2-5,11H,1H3
InChIKey
XJKWVPNWHOCFBR-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC(C=O)=CC=C1O
CAS DataBase Reference
41489-76-3
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Safety Information

HS Code 
2916399090
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Methyl 5-formyl-2-hydroxybenzoate Usage And Synthesis

Synthesis

67-56-1

616-76-2

41489-76-3

5-Formyl-2-hydroxybenzoic acid (500 g, 30 mmol, Sigma-Aldrich) was used as a raw material, mixed with concentrated H2SO4 (200 mL) and methanol (50 mL), and the reaction was stirred under reflux conditions for 24 hours. After completion of the reaction, the mixture was concentrated under reduced pressure to give 536 g of methyl 5-formyl-2-hydroxybenzoate (compound of formula FO) as a colorless oil in 99% yield.

References

[1] Patent: WO2009/27820, 2009, A2. Location in patent: Page/Page column 232
[2] Patent: US2014/155391, 2014, A1. Location in patent: Paragraph 0632; 0633
[3] Journal of Organic Chemistry, 2017, vol. 82, # 16, p. 8580 - 8589
[4] Patent: EP2143710, 2010, A1. Location in patent: Page/Page column 29
[5] Patent: EP2332942, 2011, A1. Location in patent: Page/Page column 22

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