25346-32-1

Basic information

• Product Name: 2-CHLORO-4-METHYLPENTANE
• Synonyms: 2-chloro-4-methyl-pentan;2-CHLORO-4-METHYLPENTANE;Pentane, 2-chloro-4-methyl-
• CAS NO: 25346-32-1
• Molecular Formula: C₆H₁₃Cl
• Molecular Weight: 120.62
• Mol File: 25346-32-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: -35.1°C (estimate)
• Boiling Point: 124.13°C (estimate)
• Flash Point: 20.8°C
• Appearance: /
• Density: 0.8560
• Vapor Pressure: 20.6mmHg at 25°C
• Refractive Index: 1.4093
• CAS DataBase Reference: 2-CHLORO-4-METHYLPENTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-4-METHYLPENTANE(25346-32-1)
• EPA Substance Registry System: 2-CHLORO-4-METHYLPENTANE(25346-32-1)

Safety Data

• Hazardous Substances Data: 25346-32-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H13Cl/c1-5(2)4-6(3)7/h5-6H,4H2,1-3H3

Upstream product

• 97-95-0 2-ethyl-1-butanol 
• 108-11-2 Methyl isobutyl carbinol 
• 617-48-1 malic acid 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 54942-19-7 4-hydroperoxy 2-methylpentane 
• 107-83-5 2-Methylpentane 
• 691-37-2 4-Methyl-1-pentene 

Downstream Products

• 2025-55-0 isopropyl radical 
• 187737-37-7 propene 
• 53249-18-6 1,3-dimethyl butyl radical 
• 4461-48-7 4-methyl-2-pentene 

Relevant articles and documents

USE OF COMPOSITIONS OBTAINED BY CALCINING PARTICULAR METAL-ACCUMULATING PLANTS FOR IMPLEMENTING CATALYTICAL REACTIONS

The use of metal-accumulating plants for implementing chemical reactions especially catalytical reactions.

USE OF METAL-ACCUMULATING PLANTS FOR THE PREPARATION OF CATALYSTS THAT CAN BE USED IN CHEMICAL REACTIONS

The use of metal-accumulating plants for implementing chemical reactions.

Crossover Products from Joint Reactions of Alkenes, Alkynes, and Hydrogen Halides

Joint reactions of alkenes, alkynes, and hydrogen bromide or hydrogen chloride were examined.Ethylene was the only olefin which afforded a crossed cycloadduct, viz. 1-bromo-1-methylcyclobutane (3), in its reaction with propyne and HBr.Reactions of propene with propyne/HBr, with 1-butyne/HCl, and with 2-butyne/HCl as well as reactions of 1-butene with propyne/HBr gave only cyclic and/or acyclic crossover products, which are derived from alkylation of the alkyne by the alkene.Dihalotrialkylcyclobutanes were obtained as cyclic crossover products, which had carbon skeletons composed of two molecules of the acetylene and of one molecule of the olefin used.