50671-19-7

Basic information

• Product Name: 1-(4-methylphenyl)dodecan-1-one
• Synonyms: 1-(4-methylphenyl)dodecan-1-one;1-(4-Methylphenyl)-1-dodecanone;1-p-Tolyl-1-dodecanone;4-Methyl-1-(dodecanoyl)benzene
• CAS NO: 50671-19-7
• Molecular Formula: C₁₉H₃₀O
• Molecular Weight: 274.4409
• EINECS: 256-705-0
• Mol File: 50671-19-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 380 °C at 760 mmHg
• Flash Point: 190.9 °C
• Appearance: /
• Density: 0.907 g/cm³
• Vapor Pressure: 5.62E-06mmHg at 25°C
• Refractive Index: 1.49
• CAS DataBase Reference: 1-(4-methylphenyl)dodecan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylphenyl)dodecan-1-one(50671-19-7)
• EPA Substance Registry System: 1-(4-methylphenyl)dodecan-1-one(50671-19-7)

Safety Data

• Hazardous Substances Data: 50671-19-7(Hazardous Substances Data)

Usage

General Description

1-(4-methylphenyl)dodecan-1-one is a chemical compound with the formula C19H28O. It is a ketone, characterized by a carbonyl group (C=O) bonded to a carbon atom within a 12-carbon chain. The presence of a phenyl group, which is a six-carbon aromatic ring, attached to the first carbon of the chain, gives the compound its distinctive properties. This chemical is commonly used in the manufacture of perfumes and flavorings, as it contributes to its aromatic and flavorful characteristics. Additionally, it is used in organic synthesis and as a reagent in chemical reactions due to its unique structure and properties.

InChI:InChI=1/C19H30O/c1-3-4-5-6-7-8-9-10-11-12-19(20)18-15-13-17(2)14-16-18/h13-16H,3-12H2,1-2H3

Upstream product

• 112-16-3 n-dodecanoyl chloride 
• 108-88-3 toluene 
• 143-07-7 lauric acid 
• 102020-26-8 dodecanethioic acid S-p-tolyl ester 
• 31614-66-1 tributyl(p-tolyl)stannane 
• 2050-77-3 Iododecane 
• 766-97-2 4-n-methylphenylacetylene 

Downstream Products

• 104-41-6 1-dodecyl-4-methylbenzene 
• 50671-18-6 3-Nitro-4-methyllaurophenon 
• 139512-82-6 1-(4-Bromomethyl-phenyl)-dodecan-1-one 
• 78575-44-7 1-p-Tolyl-dodecane-1,2-dione dioxime 
• 872-05-9 1-Decene 
• 139512-85-9 (4-Dodecanoyl-benzyl)-trimethyl-ammonium; bromide 
• 139512-86-0 (4-Dodecanoyl-benzyl)-triethyl-ammonium; bromide 
• 139512-87-1 (4-Dodecanoyl-benzyl)-bis-(2-hydroxy-ethyl)-methyl-ammonium; bromide 
• 50671-20-0 2-Methyl-5-lauroylanilin 
• 50671-21-1 α-(2-Chlorbenzoyl)-2-methyl-5-lauroylacetanilid 
• 50670-92-3 α-Chlor-α-(2-chlorbenzoyl)-5-lauroyl-2-methylacetanilid 

Relevant articles and documents

Iron-Catalyzed Oxyalkylation of Terminal Alkynes with Alkyl Iodides

A general oxyalkylation of terminal alkynes enabled by iron catalysis has been developed. Primary and secondary alkyl iodides acted as the alkylating reagents and afforded a range of α-alkylated ketones under mild reaction conditions. Acetyl tert-butyl peroxide (TBPA) was used as the radical relay precursor, providing the initiated methyl radical to start the radical relay process. Preliminary mechanistic studies were conducted, and late-stage functionalizations of natural product derivatives were performed.

Friedel-Crafts acylation of arenes with carboxylic acids using silica gel supported AlCl3

Aromatic compounds react smoothly with carboxylic acids in the presence of silica gel supported aluminium trichloride to afford the corresponding ketones with high regioselectivity in high to excellent yields. The catalyst is stable (as a bench top catalyst) and can be easily recovered and reused without appreciable change in its efficiency. tuebitak.

Efficient acylation of toluene and anisole with aliphatic carboxylic acids catalysed by heteropoly salt Cs2.5H0.5PW12O40

Heteropoly salt Cs2.5H0.5PW12O40 is a highly efficient and reusable solid acid catalyst for the liquid-phase acylation of toluene or anisole with C2 - C12 aliphatic carboxylic acids.