22567-38-0

Basic information

• Product Name: [S-(R*,R*)]-dihydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3(4H)-one
• Synonyms: [S-(R*,R*)]-dihydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3(4H)-one;ALPHA-BISABOLOLOXIDE;(S)-5,6-Dihydro-2,2,6-trimethyl-6-[(S)-4-methyl-3-cyclohexen-1-yl]-2H-pyran-3(4H)-one;Bisabolone oxide A;Einecs 245-087-8
• CAS NO: 22567-38-0
• Molecular Formula: C₁₅H₂₄O₂
• Molecular Weight: 236.34986
• EINECS: 245-087-8
• Mol File: 22567-38-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 320.3°Cat760mmHg
• Flash Point: 123.6°C
• Appearance: /
• Density: 0.975g/cm³
• Vapor Pressure: 0.00032mmHg at 25°C
• Refractive Index: 1.479
• CAS DataBase Reference: [S-(R*,R*)]-dihydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3(4H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: [S-(R*,R*)]-dihydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3(4H)-one(22567-38-0)
• EPA Substance Registry System: [S-(R*,R*)]-dihydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3(4H)-one(22567-38-0)

Safety Data

• Hazardous Substances Data: 22567-38-0(Hazardous Substances Data)

Usage

General Description

[S-(R*,R*)]-dihydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3(4H)-one, also known as Carveol, is a natural organic compound and a monoterpene alcohol found in the essential oils of various plants, including spearmint and caraway. It is commonly used in the production of fragrances and flavorings, as well as in the synthesis of other organic compounds. Carveol has a pleasant, minty odor and is commonly used as a flavoring agent in the food and beverage industry. It has also shown potential medicinal properties, including antioxidant and anti-inflammatory effects, and has been studied for its potential use in the treatment of various health conditions.

InChI:InChI=1/C15H24O2/c1-11-5-7-12(8-6-11)15(4)10-9-13(16)14(2,3)17-15/h5,12H,6-10H2,1-4H3

Upstream product

• 22567-36-8 [3S-[3α,6α(R^*)]]-tetrahydro-2,2,6-trimethyl-6-(4-methyl-3-cyclohexen-1-yl)-2H-pyran-3-ol 

Relevant articles and documents

On the Stereochemistry of the Bisaboloids from Matricaria chamomilla L.

The stereochemistry of the bisaboloids in chamomile - with the exception of bisabololoxide C - has been elucidated.The in-vitro-examination of the mutual convertibilities of some bisaboloids gave evidence for the stereochemical accordance of the common chiral centres of all the bisaboloids.The absolute configurations of the remaining third asymmetric carbon atoms in bisabololoxide A and B have been determined by NMR spectrometric studies in comparison with their unnatural semisynthetic epimers.All the stereogenic centres of the bisabololoxides A and B, of (-)-α-bisabolol and of bisabolonoxide A turn out to be S-configurated. - Key words: Matricaria chamomilla L., Bisaboloids, 13C NMR Spectra, Shift-Reagents