1634-09-9

Basic information

• Product Name: 11 -n-Butylnaphthalene
• Synonyms: 1-Butylnaphthalene;1-Naphthyl-1-butane; a-Butylnaphthalene
• CAS NO: 1634-09-9
• Molecular Formula: C₁₄H₁₆
• Molecular Weight: 0
• Mol File: 1634-09-9.mol
• Article Data: 40

Chemical Properties

• Boiling Point: 291.4°Cat760mmHg
• Flash Point: 131.4°C
• Appearance: /
• Density: 0.973g/cm³
• Vapor Pressure: 0.00341mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: 11 -n-Butylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 11 -n-Butylnaphthalene(1634-09-9)
• EPA Substance Registry System: 11 -n-Butylnaphthalene(1634-09-9)

Safety Data

• Hazardous Substances Data: 1634-09-9(Hazardous Substances Data)

Usage

General Description

11-n-Butylnaphthalene is a chemical compound with the molecular formula C16H16. It is a primary component in the manufacturing of heat transfer fluids, lubricants, and other specialty chemicals. 11-n-Butylnaphthalene is derived from naphthalene and butanol, and it is commonly used as a high-temperature heat transfer fluid due to its excellent thermal stability and low volatility. It also has lubricating properties and can be used as a base fluid in metalworking fluids and greases. Additionally, it is used as a chemical intermediate in the production of dyes, pharmaceuticals, and other organic compounds.

InChI:InChI=1/C14H16/c1-2-3-7-12-9-6-10-13-8-4-5-11-14(12)13/h4-6,8-11H,2-3,7H2,1H3

Upstream product

• 109-65-9 1-bromo-butane 
• 91-20-3 naphthalene 
• 90-11-9 1-Bromonaphthalene 
• 109-72-8 n-butyllithium 
• 2876-62-2 1-naphthalen-1-ylbutan-1-one 
• 3506-84-1 4-(1-naphthyl)-2-butanone 
• 92013-24-6 1-n-butyl-3,4-dihydronaphthalene 
• 542-69-8 1-iodo-butane 
• 86-53-3 1-Cyanonaphthalene 
• 109-69-3 n-Butyl chloride 
• 71-36-3 butan-1-ol 
• 693-03-8 n-butyl magnesium bromide 
• 1351445-39-0 N,N,N-trimethyl-1-naphthalenaminium trifluoromethanesulfonate 
• 86-56-6 N,N-dimethyl-1-naphthalenamine 

Downstream Products

• 38857-76-0 1-Butyl-tetralin 
• 66325-42-6 5-n-butyltetralin 

Relevant articles and documents

Fragmentation reactions of naphthalene derivatives with C4 side chains

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METHOD FOR PRODUCING ARENE COMPOUNDS AND ARENE COMPOUNDS PRODUCED BY THE SAME

Provided is a method for producing (alkyl)arene compounds represented by Formulae 3-1, 3-2, and 3-3 by the Friedel-Crafts alkylation reaction of alkyl halide compounds and arene compounds using organic phosphine compounds as a catalyst.

Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon

The palladium-catalyzed reaction of γ-silylated allyl acetates with water in the presence of CsF induces a previously unprecedented 1,2-shift of a substituent on silicon to produce allylsilanes in situ. The catalytic activity of the palladium increased when using an electron-poor phosphine ligand possessing fluorinated substituents. Further investigation of the reaction revealed that the approximate order of the migratory aptitude of groups from silicon was PhC≡C, allyl > Bn > Ph, vinyl > alkyl (Me, Et). A density functional theory study was employed to explore the reaction mechanism. Finally, the Hosomi–Sakurai-type allylation of aldehydes with in situ-generated α,γ-disubstituted allylsilanes was also investigated.