928-60-9

Basic information

• Product Name: 2-CHLORO-2-METHYLOCTANE
• Synonyms: 2-CHLORO-2-METHYLOCTANE
• CAS NO: 928-60-9
• Molecular Formula: C₉H₁₉Cl
• Molecular Weight: 162.70016
• Mol File: 928-60-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: -39.4°C (estimate)
• Boiling Point: 203.25°C (estimate)
• Flash Point: 59.934°C
• Appearance: /
• Density: 0.8739 (estimate)
• Vapor Pressure: 0.905mmHg at 25°C
• Refractive Index: 1.4207 (estimate)
• CAS DataBase Reference: 2-CHLORO-2-METHYLOCTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-2-METHYLOCTANE(928-60-9)
• EPA Substance Registry System: 2-CHLORO-2-METHYLOCTANE(928-60-9)

Safety Data

• Hazardous Substances Data: 928-60-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H19Cl/c1-4-5-6-7-8-9(2,3)10/h4-8H2,1-3H3

Upstream product

• 3761-92-0 n-hexylmagnesium bromide 
• 111-25-1 1-bromo-hexane 
• 41453-01-4 Methylniobtetrachlorid 
• 111-13-7 hexyl-methyl-ketone 
• 26533-34-6 isopropyl amyl carbinol 
• 628-44-4 2-methyl-2-octanol 

Downstream Products

• 17312-73-1 5,5-Dimethyl-undecan 
• 628-44-4 2-methyl-2-octanol 

Relevant articles and documents

α,ω-Dialkyl-Substituted Polyenes by Palladium-Catalyzed Coupling Reactions of Vinyltin Compounds with Vinyl Halides

α,ω-Dialkyl-substituted linear polyenes are synthesized in good yields by the palldium-catalyzed coupling reaction of trialkyltin- and iodo-substituted olefinic precursors.Central building blocks are the distannylated butadiene 8 and vinyl iodide 3.Our synthetic strategy was successfully applied to the preparation of the tert-butyl polyenes 13, 14, and 15 as well as polyenes 25 and 26 with longer α,ω-dialkyl chains. - Key Words: Polyenes, linear/ Vinyl tin compounds/ Vinyl halides/ Palladium catalysis

REGIOSPECIFIC AND STEREOSPECIFIC SUBSTITUTION OF HYDROXYL IN ALIPHATIC ALCOHOLS BY HALOGEN

A new system containing triphenylphosphine and trichloro- and tribromoacetic ester makes it possible to substitute the hydroxyl group in alcohols by halogen.Regiospecific and stereospecific substitution of the hydroxyl by the halogen takes place as a result of the reaction of primary and secondary aliphatic alcohols and of 2-alkenols, susceptible to isomerization processes, with this system.