2876-60-0

Basic information

• Product Name: 1-butyl naphthyl ketone
• Synonyms: 1-butyl naphthyl ketone;1-NAPHTHALEN-1-YL-PENTAN-1-ONE
• CAS NO: 2876-60-0
• Molecular Formula: C15H16O
• Molecular Weight: 212.28694
• Mol File: 2876-60-0.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 345.4 °C at 760 mmHg
• Flash Point: 148.6 °C
• Appearance: /
• Density: 1.037 g/cm³
• Vapor Pressure: 6.17E-05mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: 1-butyl naphthyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-butyl naphthyl ketone(2876-60-0)
• EPA Substance Registry System: 1-butyl naphthyl ketone(2876-60-0)

Safety Data

• Hazardous Substances Data: 2876-60-0(Hazardous Substances Data)

Usage

General Description

1-Butyl naphthyl ketone, also known as 4-phenylnaphthalen-1-yl butan-1-one, is an organic compound with the chemical formula C18H8O. It is a colorless to pale yellow liquid with a strong, sweet, floral odor. 1-Butyl naphthyl ketone is used as a fragrance ingredient in various consumer products such as perfumes, colognes, and cosmetics. It is also used as a flavoring agent in food products. Additionally, it has been used in the production of resins and plastics. However, exposure to high concentrations of 1-butyl naphthyl ketone may cause irritation to the skin, eyes, and respiratory tract, and it is considered to be a potential environmental hazard.

InChI:InChI=1/C15H16O/c1-2-3-11-15(16)14-10-6-8-12-7-4-5-9-13(12)14/h4-10H,2-3,11H2,1H3

Upstream product

• 109-72-8 n-butyllithium 
• 66821-79-2 tert-butyl naphthalene-1-carboxylate 
• 201230-82-2 carbon monoxide 
• 90-14-2 1-Iodonaphthalene 
• 15676-66-1 tri-n-butylindium 
• 638-29-9 n-valeryl chloride 
• 91-20-3 naphthalene 
• 109057-50-3 Pentaneselenoic acid Se-phenyl ester 
• 879-18-5 naphthalene-1-carbonic acid chloride 
• 86-53-3 1-Cyanonaphthalene 
• 74-88-4 methyl iodide 
• 3042-60-2 α-butyl-1-naphthalenemethanol 
• 86-55-5 1-naphthalenecarboxylic acid 
• 90-11-9 1-Bromonaphthalene 

Downstream Products

• 360-34-9 1,1,1-trifluoro-2-hexanone 
• 3007-97-4 ethyl 1-naphthoate 

Relevant articles and documents

Dearomatisation of 1- and 2-cyanonaphthalene through nucleophilic conjugate addition

Conjugate nucleophilic addition of organolithium compounds to 1- and 2-cyanonaphthalene is described for the first time. The dearomatisation is carried out in the presence of HMPA and leads to functionalised dihydronaphthalenes. The nucleophiles used incl

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.

DIHYDROIMIDAZOTHIAZOLE DERIVATIVES

Compounds of formula (I): or pharmaceutically acceptable salts thereof, exhibit 5-HT1A agonism in addition to noradrenaline reuptake inhibition and optionally also 5-HT reuptake inhibition are useful for the treatment of obesity.