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500-67-4

Product Name:Heptylresorcinol acid
Molecular Formula:C₁₃H₂₀O₂

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Product Details

Purity:99%

Global Heptylresorcinol acid 500-67-4 In Bulk Supply

500-67-4 Name
Name	Heptylresorcinol acid
Synonym	SPHEROPHORAL;1,3-Benzenediol, 5-heptyl-;5-Heptyl-1,3-benzenediol;5-HEPTYLRESORCINOL;5-Heptylbenzene-1,3-diol;5-HEPTYLRESORCINOL 95%;spherophorol;3,5-Dihydroxyheptylbenzene

500-67-4 Chemical & Physical Properties
Melting point	55-57°C
Boiling point	342.3ºC at 760 mmHg
Density	1.033 g/cm3
Molecular Formula	C13H20O2
Molecular Weight	208.29700
PSA	40.46000
LogP	3.61070
Exact Mass	208.14600
Index of Refraction	1.534

Heptylresorcinol acid 500-67-4 Usage

Heptylresorcinol acid is a natural product found in Ardisia virens with data available. The chemical formula of 5-Heptylresorcinol is C13H20O2 which containing 13 Carbon atoms,20 Hydrogen atoms and 2 Oxygen atoms, and the molecular weight of 5-Heptylresorcinol is 208.301. It is used as an antiseptic and disinfectant in topical pharmaceutical products in the treatment of skin disorders and infections. 5-Heptylresorcinol and other alkylhydroxybenzenes have been used to study the protective effect in Saccharomyces cerevisiae against oxidative and radiation-caused damage.

InChI:InChI=1/C13H20O2/c1-2-3-4-5-6-7-11-8-12(14)10-13(15)9-11/h8-10,14-15H,2-7H2,1H3

500-67-4 Relevant articles

Total syntheses of KS-501, KS-502, and their enantiomers

RG Dushin, SJ Danishefsky

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992

Chromatography of the resulting yellow oil over silica gel (eluted with 17-20% EtOAc-hexanes) gave 270 mg (99%) of the known Heptylresorcinol acid as a pale yellow oil. …

Using (+)-carvone to access novel derivatives of (+)-ent-cannabidiol: The first asymmetric syntheses of (+)-ent-CBDP and (+)-ent-CBDV

Golliher, Alexandra E.,Tenorio, Antonio J.,Dimauro, Nina O.,Mairata, Nicolas R.,Holguin, F. Omar,Maio, William

supporting information, (2021/02/20)

(?)-Cannabidiol [(?)-CBD] has recently gained prominence as a treatment for neuro-inflammation and other neurodegenerative disorders; interest is also developing in its synthetic enantiomer, (+)-CBD, which has a higher affinity to CB1/CB2 receptors than the natural stereoisomer. We have developed an inexpensive, stereoselective route to access ent-CBD derivatives using (+)-carvone as a starting material. In addition to (+)-CBD, we report the first syntheses of (+)-cannabidivarin, (+)-cannabidiphorol as well as C-6/C-8 homologues.