21948-46-9

Usage

Physical state

Colorless liquid

Odor

Strong, chloroform-like

Uses

a. Intermediate in the production of chemical compounds
b. Production of pharmaceuticals
c. Production of pesticides
d. Production of surfactants
e. Solvent
f. Manufacturing of specialty chemicals

Toxicity

Moderately toxic

Health hazards

a. Skin irritation
b. Eye irritation
c. Respiratory system irritation

Environmental impact

a. Persistence in the environment
b. Bioaccumulation in aquatic organisms
c. Potential risk to ecological systems

Handling and disposal

Caution required to prevent harm to human health and the environment

InChI:InChI=1/C8H16Cl2/c1-2-3-4-5-6-8(10)7-9/h8H,2-7H2,1H3

Upstream product

• 111-85-3 n-chlorooctane 
• 111-66-0 oct-1-ene 
• 74-85-1 ethene 
• 107-06-2 1,2-dichloro-ethane 
• 960-16-7 tributylphenylstannane 

Downstream Products

• 629-05-0 n-octyne 
• 31283-43-9 2-chloro-oct-1-ene 
• 59871-24-8 (E)-1-chlorooct-1-ene 
• 64531-23-3 1c-chloro-oct-1-ene 
• 13249-60-0 2-bromo-1-octene 
• 42843-49-2 (Z)-1-bromo-1-octene 
• 51751-87-2 (E)-1-bromo-1-octene 

Relevant academic research and scientific papers

Oxidatively intercepting heck intermediates: Pd-catalyzed 1,2- and 1,1-arylhalogenation of alkenes

This communication describes the development of two Pd-catalyzed reactions for the arylchlorination of diverse α-olefins by oxidatively intercepting Heck intermediates. Depending on the nature of the oxidant and the reaction conditions, these transformati

Polyfunctionalized N-Tensides. VII. Substitution and Elimination in the Reaction of 1,2-Dihalogenoalkanes with Amines

1,2-Dichloroalkanes, 1,2-Dibromoalkanes and mixtures of 1-bromo-2-chloroalkanes and 1-chloro-2-bromoalkanes react with primary or secondary amines and give both elimination and substitution products, often in a nearly 1:1 proportion.The elimination products are the cis and trans-1-halo-1-alkenes, the 2-halo-1-alkenes, the 1,3- and 2,4-dienes and the 1-alkenes.The main substitution products are the 1,2-bis-aminoalkanes.Physical dates, 1H-n.m.r.-spectra,surface tension values and CMC-dates are given.

MECHANISM OF RADICAL TELOMERIZATION OF ETHYLENE WITH 1,1-DICHLOROETHANE

The mechanism of the radical telomerization of ethylene with 1,2-dichloroethane was investigated. 1,2-Dichloroethane reacts with telomeric alkyl radicals with cleavage both of the C - H bond and of the C - Cl bond, and the ratio of the corresponding rate constants is 2.8 (100 deg C).It was shown that, in addition to the chlorine-containing telomers, the mixture of products from the reaction initiated by benzoyl peroxide contains alkyl- and dialkylbenzenes.