812639-15-9

Basic information

• Product Name: 1(2H)-Naphthalenone,3,4-dihydro-2-methyl-2-(2-propenyl)-,(2S)-(9CI)
• Synonyms: 1(2H)-Naphthalenone,3,4-dihydro-2-methyl-2-(2-propenyl)-,(2S)-(9CI)
• CAS NO: 812639-15-9
• Molecular Formula: C14H16O
• Molecular Weight: 0
• Product Categories: CYCLOHEXANE;METHYL
• Mol File: 812639-15-9.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1(2H)-Naphthalenone,3,4-dihydro-2-methyl-2-(2-propenyl)-,(2S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1(2H)-Naphthalenone,3,4-dihydro-2-methyl-2-(2-propenyl)-,(2S)-(9CI)(812639-15-9)
• EPA Substance Registry System: 1(2H)-Naphthalenone,3,4-dihydro-2-methyl-2-(2-propenyl)-,(2S)-(9CI)(812639-15-9)

Safety Data

• Hazardous Substances Data: 812639-15-9(Hazardous Substances Data)

Usage

General Description

1(2H)-Naphthalenone,3,4-dihydro-2-methyl-2-(2-propenyl)-,(2S)-(9CI) is a chemical compound with the molecular formula C16H16O. It is also known by the name "S(-)-β-Citronellol naphthopyran." This chemical is a derivative of β-Citronellol and is commonly used in the fragrance and flavoring industries. It has a floral and citrus-like aroma, making it a popular ingredient in perfumes, soaps, lotions, and other scented products. Additionally, it is utilized as a food additive to impart a pleasant scent and flavor in various food and beverage products. While it is generally recognized as safe for use in these applications, it is important to handle this chemical with care and to follow proper safety protocols when working with it.

Upstream product

• 1201013-85-5 C₁₅H₁₄⁽²⁾H₂O₃ 
• 1201013-83-3 C₁₅H₁₃⁽²⁾H₃O₃ 
• 460315-98-4 allyl 2-methyl-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate 
• 169825-44-9 allyl 2-methyl-3,4-dihydronaphthalen-1-yl carbonate 
• 35466-83-2 allyl methyl carbonate 
• 1590-08-5 2-methyl-1-tetralone 
• 203312-08-7 2-methyl-1-tetralone-2-carboxylic acid 
• 20907-32-8 sodium allyloxide 
• 76629-12-4 2-acetyl-2-methyl-3,4-dihydronaphthalen-1(2H)-one 
• 148624-14-0 3,4-dihydro-2-methyl-naphthalen-1-yl acetate 
• 1446139-94-1 C₁₄H₁₆O₂ 
• 107-18-6 allyl alcohol 
• 40685-04-9 1,2,3,4-tetrahydro-2-(hydroxymethylene)naphthalen-1-one 
• 91962-77-5 2-methyl-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carbaldehyde 

Relevant articles and documents

Palladium-catalyzed asymmetric alkylation of ketone enolates [7]

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Phosphination of Phenol Derivatives and Applications to Divergent Synthesis of Phosphine Ligands

We describe a general and efficient protocol for the synthesis of organophosphine compounds from phenols and phosphines (R2PH) via a metal-free C-O bond cleavage and C-P bond formation process. This approach exhibits broad substrate scope and excellent functional group tolerance. The synthetic utilities of this protocol were demonstrated by the synthesis of chiral ligands via the various transformations of cyano groups and their applications in asymmetric catalysis.

Enol Acetates: Versatile Substrates for the Enantioselective Intermolecular Tsuji Allylation

A highly versatile enantioselective intermolecular Tsuji allylation that generates alpha-quaternary stereocenters is reported. The methodology utilizes a prochiral enol acetate as a substrate, which is the last class of the original Tsuji substrates to be