2,4-dihydroxy-6-propyl-benzoic acid methyl ester
2,4-dihydroxy-6-propyl-benzoic acid methyl ester Basic information
- Product Name:
- 2,4-dihydroxy-6-propyl-benzoic acid methyl ester
- Synonyms:
-
- 2,4-dihydroxy-6-propyl-benzoic acid methyl ester
- methyl 2,4-dihydroxy-6-propylbenzoate
- 2,4-dihydroxy-6-n-propylbenzoic acid, methyl ester
- Benzoic acid, 2,4-dihydroxy-6-propyl-, methyl ester
- Methyl divatate
- Methyl Divarinolcarboxylate
- 4-dihydroxy-6-propylbenzoate
- 2,4-dihydroxy-6-propyl-benzoic acid methyl
- CAS:
- 55382-52-0
- MF:
- C11H14O4
- MW:
- 210.23
- EINECS:
- 810-694-4
- Mol File:
- 55382-52-0.mol
2,4-dihydroxy-6-propyl-benzoic acid methyl ester Chemical Properties
- Boiling point:
- 388.6±27.0 °C(Predicted)
- Density
- 1.211±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 8.27±0.23(Predicted)
- InChI
- InChI=1S/C11H14O4/c1-3-4-7-5-8(12)6-9(13)10(7)11(14)15-2/h5-6,12-13H,3-4H2,1-2H3
- InChIKey
- AREDPURTHQTRTK-UHFFFAOYSA-N
- SMILES
- C(OC)(=O)C1=C(CCC)C=C(O)C=C1O
2,4-dihydroxy-6-propyl-benzoic acid methyl ester Usage And Synthesis
Description
2,4-dihydroxy-6-propyl-benzoic acid methyl ester is a carboxylate derivative and can be used as a pharmaceutical intermediate.
Chemical Properties
Pale yellow solid.
Uses
Methyl Divarinolcarboxylate is used in methods of manufacturing Cannabidiol or Cannabidivarin.
Definition
2,4-dihydroxy-6-propyl-benzoic acid methyl ester is a natural product found in Lobaria scrobiculata and Lobarina scrobiculata with data available.
Preparation
2,4-Dihydroxy-6-propylbenzoic acid was dissolved in methanol, and then a catalytic amount (a few drops) of concentrated sulfuric acid was added. The esterification reaction took place, followed by removal of the solvent. The resulting crude product was dissolved in ethyl acetate. The ethyl acetate solution was washed with water and then with saline. The organic layer was then dried using magnesium sulfate. The product was concentrated and subjected to purification using silica gel column chromatography. Finally, product A was obtained after the purification process.
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