334-56-5

Basic information

• Product Name: 1-FLUORODECANE
• Synonyms: 1-FLUORODECANE;N-DECYL FLUORIDE;1-fluoro-decan;Decyl fluoride;decylfluoride;1-Fluorodecane98%;Decyl fluoride 98%
• CAS NO: 334-56-5
• Molecular Formula: C₁₀H₂₁F
• Molecular Weight: 160.27
• EINECS: 206-380-6
• Product Categories: Alkyl;Building Blocks;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks
• Mol File: 334-56-5.mol
• Article Data: 19

Chemical Properties

• Melting Point: -35°C
• Boiling Point: 185-187 °C(lit.)
• Flash Point: 175 °F
• Appearance: /
• Density: 0.809 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.927mmHg at 25°C
• Refractive Index: n20/D 1.409(lit.)
• CAS DataBase Reference: 1-FLUORODECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-FLUORODECANE(334-56-5)
• EPA Substance Registry System: 1-FLUORODECANE(334-56-5)

Safety Data

• Hazard Codes: T+,N,F
• Statements: 28-50/53
• Safety Statements: 28-36/37-45-60-61
• RIDADR: UN 2810 6.1/PG 1
• WGK Germany: 3
• RTECS: HD8575000
• Hazardous Substances Data: 334-56-5(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 43, p. 3173, 1965 DOI: 10.1139/v65-442

InChI:InChI=1/C10H21F/c1-2-3-4-5-6-7-8-9-10-11/h2-10H2,1H3

Upstream product

• 41233-29-8 methanesulfonic acid decyl ester 
• 5509-08-0 decyl p-toluenesulfonate 
• 2050-77-3 Iododecane 
• 112-30-1 1-Decanol 
• 20157-33-9 n-decylmagnesium chloride 
• 90238-20-3 N,N-diethyl-α,α-difluorobenzylamine 
• 110-53-2 1-Bromopentane 
• 4665-35-4 2-decyl-1,1-diphenyl-isourea; hydrofluoride 
• 112-29-8 1-bromo dodecane 
• 1002-69-3 decyl chloride 

Downstream Products

• 112-40-3 dodecane 
• 104-72-3 decylbenzene 
• 124-18-5 decane 
• 25727-94-0 4-decylmorpholine 
• 30189-87-8 N-decyl-N-methylaniline 
• 64154-08-1 2-iododecane 
• 2050-77-3 Iododecane 
• 768-93-4 1-iodoadamantane 
• 111-65-9 octane 
• 111-84-2 nonane 
• 59386-47-9 2-decylcyclohexanone 
• 4537-13-7 2-phenyldecane 
• 4537-11-5 (1-butylhexyl)benzene 
• 1198605-32-1 [HPMes₃][B(C₆F₅)4] 

Relevant articles and documents

DARSTELLUNG VON PRIMAEREN ALKYLFLUORIDEN UNTER EINSATZ DER PHASEN TRANSFER KATALYSE

The influence of the following factors on the solid-liquid PTC fluorination reaction of primary alkyl halides was studied: the catalyst quantity applied, the water content of solid alkali fluoride salt, and the type of catalyst.Kinetic curves at different temperatures were found for the reaction.The maximum yield is a function of the interaction of two parallel running reactions, namely the direct fluorination reaction and the catalyst decomposition.

Synthesis, Characterization, and Reactivity of Thermally Stable Anhydrous Quaternary Ammonium Fluorides

The synthesis and properties of a new class of anhydrous quaternary ammonium fluorides, based on the rigid skeleton azabicyclo[2.2.2]octane, is described. Compounds 2a-d were easily prepared by passing the corresponding ammonium iodides over fluoride-based resin followed by drying their hydrated form at 100 or 140 °C under reduced pressure. The stability (experimental and theoretical study), solubility, reactivity, and characterization by solution and solid-state MAS NMR are discussed.

Selective mono-acylation of 1,2- and 1,3-diols using (α,α- difluoroalkyl)amines

In the reaction of N,N-diethyl-α,α-difluorobenzylamine (DFBA) with 1,2- or 1,3-diols, selective mono-benzoylation occurs to afford mono-esters of the diols in good yield. The reaction is completed under mild conditions in a short reaction time. Further, prim-, sec-, and tert-diols and catechol can be converted to the corresponding mono-benzoates. DFBA is used for the protection of the hydroxy group in sugars. The selective mono-nicotinylation, formylation and pivaloylation of diols are also performed by using the corresponding difluoroalkylamines.