871-90-9

Basic information

• Product Name: 8-Chloro-1-octene
• Synonyms: Oct-7-en-1-yl chloride
• CAS NO: 871-90-9
• Molecular Formula: C₈H₁₅Cl
• Molecular Weight: 146.66
• Mol File: 871-90-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 180.9°C at 760 mmHg
• Flash Point: 59.1°C
• Appearance: /
• Density: 0.877g/cm³
• Vapor Pressure: 1.19mmHg at 25°C
• Refractive Index: 1.436
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 8-Chloro-1-octene(CAS DataBase Reference)
• NIST Chemistry Reference: 8-Chloro-1-octene(871-90-9)
• EPA Substance Registry System: 8-Chloro-1-octene(871-90-9)

Safety Data

• Hazardous Substances Data: 871-90-9(Hazardous Substances Data)

Usage

General Description

8-Chloro-1-octene is an organic compound and a member of the alkene family of hydrocarbons. It has the chemical formula C8H15Cl and is derived from 1-octene, with a chlorine atom substituted at the 8th carbon position. It is commonly used as a starting material in the synthesis of various chemical compounds, including pharmaceuticals, agrochemicals, and polymers. 8-Chloro-1-octene is a versatile intermediate chemical that can undergo various reactions to produce a wide range of products, making it valuable in the chemical industry. It is also used as a research chemical in laboratories for studying organic synthesis and reaction mechanisms.

InChI:InChI=1/C8H15Cl/c1-2-3-4-5-6-7-8-9/h2H,1,3-8H2

Upstream product

• 24088-97-9 8-chloro-oct-1-yne 
• 107-05-1 3-chloroprop-1-ene 
• 628-76-2 1,5-dichloropentane 
• 1730-25-2 allylmagnesium bromide 
• 54512-75-3 1-bromo-5-chloropentane 
• 2622-05-1 allylmagnesium bromide 
• 6294-17-3 1-bromo-6-chlorohexane 
• 75-01-4 chloroethylene 
• 13175-44-5 oct-7-en-1-ol 
• 106-95-6 allyl bromide 

Downstream Products

• 38380-55-1 8-iodo-oct-1-ene 
• 23144-52-7 8-chlorooctan-1-ol 
• 110683-61-9 4-(7-octenyloxy)benzoic acid 
• 103177-38-4 8-[p-(7-octenyloxy)benzoyl]amino-2-(5-tetrazolyl)-4-oxo-4H-1-benzopyran 
• 103176-89-2 4-Oct-7-enyloxy-N-[3-(1H-tetrazol-5-yl)-2,3-dihydro-benzo[1,4]dioxin-5-yl]-benzamide 

Relevant articles and documents

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We devise a new and green route for the multi-gram synthesis of core–shell nanoparticles (NPs) in one step under organic-free and pH-neutral conditions. Simply mixing core and shell metal precursors in the presence of solid metal oxides in water allowed for the facile fabrication of small CeO2-covered Au and Ag nanoparticles dispersed on metal oxides in one step. The CeO2-covered Au nanoparticles acted as a highly efficient and reusable catalyst for a series of chemoselective hydrogenations, while retaining C=C bonds in diverse substrates. Consequently, higher environmental compatibility and more efficient energy savings were achieved across the entire process, including catalyst preparation, reaction, separation, and reuse.

METHOD FOR PRODUCING UNSATURATED GROUP-CONTAINING HALIDE

PROBLEM TO BE SOLVED: To provide a method for producing an unsaturated group-containing halide whereby an unsaturated group-containing halide expected or used as an intermediate in the fields of medicine, agrochemical, resin and the like can be produced by a safe method, easily and at good yields. SOLUTION: The present invention provides a method for producing an unsaturated group-containing halide represented by formula (3) by halogenating an unsaturated group-containing alcohol represented by formula (2), in the presence of an organic base, with a sulfonic acid halide as a halogenating agent [R2 and R3 are H or unsubstituted; n is an integer of 1-6; and an unsaturated bond is a double bond or a triple bond]. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

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