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Postion:Product Catalog >Organic Chemistry>Alcohols,Phenols,Phenol alcohols>5-Propyl-1,3-benzenediol
5-Propyl-1,3-benzenediol
  • 5-Propyl-1,3-benzenediol
  • 5-Propyl-1,3-benzenediol
  • 5-Propyl-1,3-benzenediol
  • 5-Propyl-1,3-benzenediol

5-Propyl-1,3-benzenediol

Price Get Latest Price
Package 1KG
Min. Order: 0.1KG
Supply Ability: 1000KGS
Update Time: 2024-08-15

Product Details

Product Name: 5-Propyl-1,3-benzenediol CAS No.: 500-49-2
Min. Order: 0.1KG Purity: 98%
Supply Ability: 1000KGS Release date: 2024/08/15

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5-Propyl-1,3-benzenediol Basic information
Product Name:5-Propyl-1,3-benzenediol
Synonyms:5-Propyl-1,3-benzenediol;Divarinol;1,3-Benzenediol, 5-propyl-;3,5-Dihydroxypropylbenzene;1,3-Benzenediol, 5-propyl- CAS NO.500-49-2;3,5-Dihydroxy-1-propylbenzene
CAS:500-49-2
MF:C9H12O2
MW:152.19
EINECS:
Product Categories:
Mol File:500-49-2.mol
Article illustration

5-Propyl-1,3-benzenediol Chemical PropertiesMelting point 82.8°CBoiling point 234.66°C (rough estimate)density 1.0505 (rough estimate)refractive index 1.4024 (estimate)solubility DMF: 2 mg/ml; DMSO: 2 mg/ml; Ethanol: 5 mg/ml; PBS (pH 7.2): 1 mg/mlform A crystalline solidpka9.56±0.10(Predicted)

Safety InformationHS Code 2907290090
MSDS Information

5-Propyl-1,3-benzenediol Usage And SynthesisDescriptionA White to Brown crystalline solid.Uses5-Propylbenzene-1,3-diol is an intermediate used to prepare Cannabigerovarin (C175140) which stimulates thermosensitive transient receptor potential (TRP) channels of vanilloid type-4 (TRPV4)-mediated [Ca2+]i with moderate-high efficacy (30-60% of the effect of ionomycin) and potency (EC50 0.9-6.4 μM),SynthesisIn a 100 mL round bottom flask, open to the atmosphere was added the crude product Benzene, 1,3-dimethoxy-5-propyl (0.736 g, 4.08 mmol, 1.0 equiv.) and a 1:1 mixture of glacial acetic acid (20 mL, 349.7 mmol, 17.4 M) and hydrobromic acid (48% in H2O, 20 mL, 368.3 mmol, 18.4 M). The reaction mixture was refluxed at 125 °C for 3 hours while stirring, or until the starting material was consumed via TLC analysis. At this point, the reaction was allowed to cool to room temperature and quenched by the addition of DI H2O. The biphasic solution was added to a separatory funnel, wherein the organic portion was extracted Et2O (ca. 3x 20 mL). The organic layers were then combined, neutralized with a concentrated sodium bicarbonate solution (ca. 30 mL), washed with a saturated brine solution (ca. 50 mL), dried over MgSO4, filtered, and concentrated in vacuo to afford the final product without 5-Propyl-1,3-benzenediol (0.609 g, 99% yield) as a pale yellow oil.
Article illustrationSolubility in organics5-Propyl-1,3-benzenediol is soluble in N,N-dimethylformamide, soluble in methanol, slightly soluble in glacial acetic acid, very slightly soluble in chloroform, almost insoluble in water.


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