32676-16-7

Basic information

• Product Name: dihydroperillic acid
• Synonyms: dihydroperillic acid
• CAS NO: 32676-16-7
• Molecular Formula: C₁₀H₁₆O₂
• Molecular Weight: 168.23
• Mol File: 32676-16-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 275.9°Cat760mmHg
• Flash Point: 131.1°C
• Appearance: /
• Density: 1.024g/cm³
• Vapor Pressure: 0.00135mmHg at 25°C
• Refractive Index: 1.486
• CAS DataBase Reference: dihydroperillic acid(CAS DataBase Reference)
• NIST Chemistry Reference: dihydroperillic acid(32676-16-7)
• EPA Substance Registry System: dihydroperillic acid(32676-16-7)

Safety Data

• Hazardous Substances Data: 32676-16-7(Hazardous Substances Data)

Usage

Description

Dihydroperillic acid, also known as 1,2-dihydroperillic acid, is a chemical compound with potential anticancer properties. It is currently being studied in phase I clinical trials for its effectiveness in treating cancer patients.

Uses

Used in Oncology:
Dihydroperillic acid is used as an anticancer agent in phase I studies for the treatment of cancer patients. It is being evaluated for its potential to target and inhibit the growth of cancer cells, offering a new therapeutic option for cancer treatment.

InChI:InChI=1/C10H16O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h8-9H,1,3-6H2,2H3,(H,11,12)

Upstream product

• 7694-45-3 4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid 
• 71-41-0 pentan-1-ol 
• 536-59-4 (-)-perillyl alcohol 

Relevant articles and documents

Oxidative Transformations of Biosourced Alcohols Catalyzed by Earth-Abundant Transition Metals

The catalytic acceptorless dehydrogenative oxidation of biosourced alcohols into carboxylic acid salts was achieved using earth-abundant Fe and Mn complexes that feature aliphatic PNP pincer ligands in good to excellent yields. The Fe derivatives were characterized by using 57Fe NMR spectroscopy. Mn pincer catalysts are catalytically more efficient than their Fe counterparts thanks to their robustness under basic conditions. Attempts to generate aldehydes from alcohols were not successful using the Fe and Mn species, but a commercially available Ru analogue achieves this transformation selectively under very mild conditions in the presence of a large excess of acetone as a hydrogen acceptor.