124688-07-9

Basic information

• Product Name: 2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE
• Synonyms: 2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE
• CAS NO: 124688-07-9
• Molecular Formula: C12H14O2
• Molecular Weight: 190.24
• Mol File: 124688-07-9.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE(124688-07-9)
• EPA Substance Registry System: 2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE(124688-07-9)

Safety Data

• Hazardous Substances Data: 124688-07-9(Hazardous Substances Data)

Usage

Bicyclic ketone

It is a bicyclic ketone, meaning it has a structure composed of two interconnected rings, with one of the rings containing a carbonyl group (C=O).

Methoxy group

A methoxy group (-OCH3) is attached to the six-membered ring in the compound, which contributes to its aromatic properties.

Sweet, floral, and woody aroma

2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE is known for imparting a sweet, floral, and woody aroma, making it a popular choice in the fragrance and flavor industry.

Common uses in perfumes and colognes

The compound is widely used in the production of perfumes, colognes, and other scented products due to its pleasant aroma.

Potential applications in pharmaceuticals

2,3-DIHYDRO-2,2-DIMETHYL-6-METHOXY-1H-INDEN-1-ONE may have potential applications in the pharmaceutical industry, although its specific uses and health effects are not yet fully understood.

Proper handling and disposal

Due to the potential health effects and environmental impact of this chemical compound, it is important to follow proper handling and disposal procedures in accordance with local regulations.

Upstream product

• 6026-75-1 1-(3-methoxyphenyl)-2-methyl-propan-1-one 
• 1355253-97-2 C₁₅H₂₄O₂Si 
• 13623-25-1 6-methoxy-2,3-dihydro-1H-inden-1-one 
• 74-88-4 methyl iodide 

Downstream Products

• 165072-41-3 6-methoxy-2,2-dimethyl-2,3-dihydro-1H-indene-1-ol 

Relevant articles and documents

Silylative Kinetic Resolution of Racemic 2,2-Dialkyl 5- and 6-Membered Cyclic Benzylic Alcohol Derivatives Catalyzed by Chiral Guanidine, (R)-N-Methylbenzoguanidine

Efficient silylative kinetic resolution of racemic 2,2-dialkyl 5- and 6-membered cyclic benzylic alcohols was achieved using diphenylmethylchlorosilane (Ph2MeSiCl) or phenyldimethylchlorosilane (PhMe2SiCl) as a silyl source catalyzed by chiral guanidine. The reaction could be applied to a broad range of 2,2-dialkyl 1-indanols with good s-values, irrespective of the electronic nature of the substituent on the aromatic ring of the substrates and the type of substituent at the C2-position. In addition, several 2,2-dimethyl 6-membered cyclic and heterocyclic alcohols could be adopted in the reaction. (Figure presented.).

Synthesis of α-indanones via intramolecular direct arylation with cyclopropanol-derived homoenolates

A palladium-catalysed, tandem cyclopropanol rearrangement and direct arylation approach for the synthesis of 1-indanones is reported. The reaction is generally high yielding, uses oxygen as the terminal oxidant and tolerates a range of functional groups on the aryl ring.

Benzocycloalkene compounds, their production and use

A compound of the formula wherein R1and R2are H, a hydrocarbon group or a heterocyclic group, or R1and R2are combinedly a spiro ring; R3is a hydrocarbon group, a substituted amino group, a substituted