23733-65-5

Basic information

• Product Name: (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one
• Synonyms: (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one;(R)-6-Methyl-3-(1-methylethyl)-2-cyclohexen-1-one;2-Cyclohexen-1-one, 6-methyl-3-(1-methylethyl)-, (R)-(+)-;Einecs 245-850-5
• CAS NO: 23733-65-5
• Molecular Formula: C₁₀H₁₆O
• Molecular Weight: 152.23344
• EINECS: 245-850-5
• Mol File: 23733-65-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 234.5°Cat760mmHg
• Flash Point: 90.9°C
• Appearance: /
• Density: 0.915g/cm³
• Refractive Index: 1.464
• CAS DataBase Reference: (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one(23733-65-5)
• EPA Substance Registry System: (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one(23733-65-5)

Safety Data

• Hazardous Substances Data: 23733-65-5(Hazardous Substances Data)

Usage

General Description

(R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one is a chemical compound with a molecular formula of C10H16O. It is a cyclic enone that consists of a cyclohexene ring with an isopropyl group and a methyl group attached to it. (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one is commonly used as a flavoring agent in the food and beverage industry due to its aromatic and fruity odor. It is also used in the production of fragrances and as a starting material in the synthesis of other organic compounds. Additionally, (R)-3-(isopropyl)-6-methylcyclohex-2-en-1-one has potential applications in pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity.

InChI:InChI=1/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h6-8H,4-5H2,1-3H3/t8-/m1/s1

Upstream product

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Relevant articles and documents

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Molecular rearrangements of α-(trans)- and β-(cis)-3,4-epoxycaranes in acid media

Configuration of the oxirane ring in stereoisomeric 3,4-epoxycaranes affects the direction of their skeletal rearrangements in liquid (HSO3F-SO2FCl) and over solid (TiO2/SO42-) superacids; in the latter case, compounds postulated as intermediates in the liquid-phase process have been isolated.

REARRANGEMENT OF TERPENOIDS WITH BORON TRIFLUORIDE ETHERATE

The details of the rearrangement of some isopimaranes in the presence of boron trifluoride etherate are presented and explained.As a result of comparative studies with terpenoids in the presence of BF3, it is proposed that the complex of this Lewis acid with ketones acts as a Bronsted acid in the equilibration of double bonds.It is also suggested that natural products with the carbon skeleton of the rearrangement product should be encountered in nature.