1686-54-0

Basic information

• Product Name: 13β-Methyl-13-vinylpodocarp-8(14)-en-18-oic acid methyl ester
• Synonyms: 13β-Methyl-13-vinylpodocarp-8(14)-en-18-oic acid methyl ester;Methyl sandaracopimarate
• CAS NO: 1686-54-0
• Molecular Formula: C₂₁H₃₂O₂
• Molecular Weight: 316.47758
• Mol File: 1686-54-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 61.5-62 °C
• Boiling Point: 380.6±42.0 °C(Predicted)
• Appearance: /
• Density: 1.01±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 13β-Methyl-13-vinylpodocarp-8(14)-en-18-oic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 13β-Methyl-13-vinylpodocarp-8(14)-en-18-oic acid methyl ester(1686-54-0)
• EPA Substance Registry System: 13β-Methyl-13-vinylpodocarp-8(14)-en-18-oic acid methyl ester(1686-54-0)

Safety Data

• Hazardous Substances Data: 1686-54-0(Hazardous Substances Data)

Usage

Natural Occurrence

Found in certain plant species.

Chemical Family

Belongs to the family of podocarpic acid derivatives.

Pharmaceutical and Medicinal Applications

Commonly used in the pharmaceutical and medicinal industry.

Anti-Inflammatory Properties

Studied for its potential anti-inflammatory properties.

Anti-Cancer Properties

Investigated for its potential anti-cancer properties.

Immune Response Modulation

Has been studied for its role in modulating the immune response.

Research Synthesis

Used in the synthesis of various organic compounds for research purposes.

Potential Lead Compound

Shows promise as a potential lead compound for the development of new drugs and therapies.

Pharmaceutical and Medicinal Promise

Holds significant promise for various pharmaceutical and medicinal applications due to its diverse and valuable properties.

Upstream product

• 471-74-9 sandaracopimaric acid 
• 186581-53-3 diazomethane 

Downstream Products

• 3855-14-9 sandaracopimarinal 
• 124062-64-2 methyl 16-tert-butyldiphenylsyloxy-13-epi-pimar-8⁽¹⁴⁾-en-18-oate 
• 1686-61-9 sandaracopimaradiene 
• 163456-10-8 methyl 14-oxo-16-triphenylmethoxy-8α-isopimarate 
• 163456-11-9 methyl 14-oxo-16-(triphenylmethoxy)isopimarate 
• 163456-12-0 methyl 14β-hydroxy-16-(triphenylmethoxy)isopimarate 
• 163456-09-5 methyl 4α-hydroxy-16-triphenylmethoxy-8α-isopimarate 
• 33952-78-2 Methyl-isopimar-8-en-18-oat 
• 3867-54-7 methyl 15,16-dihydro-13-epi-pimar-8(14)-en-18-oate 
• 19907-21-2 Methyl isopimara-8,15-dien-18-oate 
• 24563-84-6 sandaracopimara-8⁽¹⁴⁾,15-dien-18-ol 

Relevant articles and documents

PART I. EPOXYDES DITERPENIQUES : SYNTHESE ET REACTIVITE D'EPOXYDES DERIVES D'ACIDES RESINIQUES

Epoxidation of methyl esters of resin acids with the pimarane skeleton with p-nitroperbenzoic acid has permitted the isolation of epoxides of the intracyclic double bond.Allylic diterpenic alcohols were obtained by acid-catalysed isomerisation of diterpene epoxides, and the action of Collins reagent on these allylic alcohols has been studied.

METABOLITES OF THE HONEY MUSHROOM, Armillaria mellea

The fungus Armillaria mellea (Vahl ex.Fr.) Kummer is responsible for severe losses in timber and fruit production.The metabolites isolated when certain strains of this fungus are grown in liquid culture have been identified as diterpenoid acids posessing the abietane (1) and pimarane (2) skeletons.These compounds, known collectively as resin acids, have not been reported previously from fungal source.In addition to the resin acids dehydroabietic acid (3), pimaric acid (4), isopimaric acid (5), and sandaracopimaric acid (6), three additional acids, levopimaric acid endo-peroxide (7), 7-oxodehydroabietic acid (9), and 7-oxo-15-hydroxydehydroabietic acid (10) were obtained.On one accasion three orange pigments, austocystin F (11), averufin (12), and averufanin (13), all previously known fungal metabolites, were isolated.