40061-88-9

Basic information

• Product Name: 12-(acetyloxy)podocarpa-8,11,13-trien-15-oic acid
• CAS NO: 40061-88-9
• Molecular Formula: C₁₉H₂₄O₄
• Molecular Weight: 316.3915
• Mol File: 40061-88-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 458.5°C at 760 mmHg
• Flash Point: 160.9°C
• Density: 1.166g/cm³
• Vapor Pressure: 3.36E-09mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: 12-(acetyloxy)podocarpa-8,11,13-trien-15-oic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 12-(acetyloxy)podocarpa-8,11,13-trien-15-oic acid(40061-88-9)
• EPA Substance Registry System: 12-(acetyloxy)podocarpa-8,11,13-trien-15-oic acid(40061-88-9)

Safety Data

• Hazardous Substances Data: 40061-88-9(Hazardous Substances Data)

Usage

Chemical compound

A substance formed by the chemical combination of two or more elements in a fixed proportion.

Derived from podocarpus plant

The compound is sourced from the podocarpus plant, which belongs to the Podocarpaceae family.

Diterpenoid

A type of organic compound found in various plants, characterized by a specific carbon skeleton structure.

Contains an acetyloxy group

The compound has an acetyl group attached to it, which is a functional group derived from acetic acid.

Chemical properties

The presence of the acetyloxy group influences the compound's reactivity, solubility, and other chemical behaviors.

Potential biological activities

The compound may exhibit various biological effects, such as anti-inflammatory, anticancer, and antimicrobial properties.

Pharmacological effects

The compound's potential therapeutic uses are being studied, including its effects on the immune system and cancer cells.

Further research needed

More research is required to fully understand the compound's potential uses, effects, and mechanisms of action.

Structure

The compound has a specific molecular structure, with a carbon skeleton consisting of four isoprene units.

Solubility

The compound's solubility in various solvents may be influenced by the presence of the acetyloxy group.

Stability

The compound's stability under different conditions, such as temperature and pH, may be affected by its functional groups.

Synthesis

The compound can be synthesized through various chemical reactions, involving the formation of the acetyloxy group and the assembly of the diterpenoid skeleton.

Extraction

The compound can be extracted from the podocarpus plant using various extraction techniques, such as solvent extraction or steam distillation.

Purification

The compound may need to be purified after extraction to remove impurities and obtain a pure sample for further study.

Analysis

Various analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, can be used to characterize and confirm the structure of the compound.

Upstream product

• 5947-49-9 podocarpic acid 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Relevant articles and documents

212. Significance of the Geminal Dimethyl Group in the Odor Principle of Ambrox

The diastereoisomeric 18-nor- and 19-norambrox ((6α)- and (6β)-dodecahydro-3a,6,9a-trimethylnaphtholfurans resp.) as well as the corresponding 18,19-dinor-derivatives (dodecahydro-3a,9a-dimethylnaphthofurans) have been synthesized and subjected to sensory evaluation.Threshold data and odor determination give an enlarged insight into the structure-activity relationship (SAR) in ambrox-type ambergris fragrances.As a general conclusion, the accumulation of axial CH3 groups in the tricyclic ethers 1-12 leads to the strongest receptor affinity.