94530-80-0

Basic information

• Product Name: 1-Propanone,3-phenyl-1-[2,4,6-trihydroxy-3-[(1R,6R)-3-methyl-6-(1-methylethyl)-2-cyclohexen-1-yl]phenyl]-
• CAS NO: 94530-80-0
• Molecular Formula: C25H30 O4
• Molecular Weight: 394.511
• Mol File: 94530-80-0.mol

Chemical Properties

• CAS DataBase Reference: 1-Propanone,3-phenyl-1-[2,4,6-trihydroxy-3-[(1R,6R)-3-methyl-6-(1-methylethyl)-2-cyclohexen-1-yl]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone,3-phenyl-1-[2,4,6-trihydroxy-3-[(1R,6R)-3-methyl-6-(1-methylethyl)-2-cyclohexen-1-yl]phenyl]-(94530-80-0)
• EPA Substance Registry System: 1-Propanone,3-phenyl-1-[2,4,6-trihydroxy-3-[(1R,6R)-3-methyl-6-(1-methylethyl)-2-cyclohexen-1-yl]phenyl]-(94530-80-0)

Safety Data

• Hazardous Substances Data: 94530-80-0(Hazardous Substances Data)

Usage

Molecular Structure

Complex The compound has a long and specific molecular structure, which includes a propanone group, a phenyl group, a cyclohexenyl group, and a trihydroxy structure.

Functional Groups

Propanone, Phenyl, Cyclohexenyl, Trihydroxy The compound contains various functional groups that contribute to its chemical properties and reactivity.

Stereochemistry

(1R,6R) The compound has specific stereochemistry, which affects its spatial arrangement and interactions with other molecules.

Potential Applications

Organic Synthesis, Pharmaceuticals Due to its intricate structure and potential reactivity, the chemical may have various applications in organic synthesis, pharmaceuticals, and other industries.

Research and Analysis

Necessary Further research and analysis are required to fully understand the properties and potential uses of this complex compound.

Upstream product

• 98155-84-1 linderatone 
• 1088-08-0 2',4',6'-trihydroxydihydrochalcone 
• 4221-98-1 (R)-5-isopropyl-2-methylcyclohexa-1,3-diene 

Downstream Products

• 67831-93-0 1-(3,5-Dihydroxy-12-isopropyl-9-methyl-8-oxa-tricyclo[7.3.1.0^2,7]trideca-2⁽⁷⁾,3,5-trien-4-yl)-3-phenyl-propan-1-one 

Relevant articles and documents

REVISED STRUCTURES OF LINDERATONE AND METHYLLINDERATONE

The structure of a terpenylflavanone, linderatone, was revised to 6-terpenylflavanone by 1H-13C long-range cosy experiment.Therefore, the structure of methyllinderatone was also revised to 4.

Terpenylations Using (R)-(-)-α-Phellandrene. Synthesis of the (3S,4R)-8,9-Dihydro-o- and -p-cannabidiols, their iso-THC's, and the Natural Dihydrochalcone (3S,4R)-(+)-Linderatin

Catalysed by toluene-p-sulphonic acid at 5 deg C, (R)-(-)-α-phellandrene reacts with olivetol to give (3S,4R)-8,9-dihydro-p- and -o-cannabidiols.At 80 deg C under the acid conditions the latter retrogresses substantially to the former and both cyclise giv