53155-10-5

Basic information

• Product Name: (E)-1-Bromo-3-octene
• Synonyms: (E)-1-Bromo-3-octene
• CAS NO: 53155-10-5
• Molecular Formula: C₈H₁₅Br
• Molecular Weight: 191.11
• Mol File: 53155-10-5.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 198.4°C at 760 mmHg
• Flash Point: 70.4°C
• Appearance: /
• Density: 1.141g/cm³
• Vapor Pressure: 0.508mmHg at 25°C
• Refractive Index: 1.472
• CAS DataBase Reference: (E)-1-Bromo-3-octene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-Bromo-3-octene(53155-10-5)
• EPA Substance Registry System: (E)-1-Bromo-3-octene(53155-10-5)

Safety Data

• Hazardous Substances Data: 53155-10-5(Hazardous Substances Data)

Usage

Description

(E)-1-Bromo-3-octene, with the molecular formula C8H15Br, is an organic compound featuring a carbon chain of eight atoms with a double bond between the first and second carbons and a bromine atom attached to the first carbon. This molecule is known for its high reactivity and sensitivity to air and moisture, necessitating careful handling in a controlled environment.

Uses

Used in Organic Synthesis:
(E)-1-Bromo-3-octene is utilized as a key intermediate in the production of a variety of chemicals, including pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Chemical Research and Development:
As a building block for the synthesis of other organic compounds, (E)-1-Bromo-3-octene serves as an important tool in the field of chemical research and development. Its versatility in forming new compounds contributes to the advancement of chemical knowledge and the creation of novel substances with potential applications across various industries.

InChI:InChI=1/C8H15Br/c1-2-3-4-5-6-7-8-9/h5-6H,2-4,7-8H2,1H3/b6-5+

Upstream product

• 91408-00-3 trans-1-cyclopropyl-2-penten-1-one 
• 127934-19-4 1-cyclopropyl-3-trimethylsilyloxypentanone 
• 35234-16-3 (E)-methyl oct-3-enoate 
• 18185-81-4 cis-3-octen-1-ol 
• 126629-19-4 C₁₁H₁₈O₄ 
• 5163-67-7 (E)-oct-3-enoic acid 
• 14113-86-1 1-cyclopropyl-1-pentanone 
• 14916-80-4 oct-3-yn-1-ol 
• 111789-39-0 (Z)-oct-3-enyl 4-methylbenzenesulfonate 
• 4379-16-2 1-cyclopropylpentan-1-ol 
• 18185-81-4 (E)-oct-3-en-1-ol 
• 693-03-8 n-butyl magnesium bromide 
• 38771-21-0 4-bromobut-1-yne 

Downstream Products

• 35602-33-6 (3E)-octenyl acetate 
• 53963-09-0 (7Z,11E)-hexadeca-7,11-dien-1-ol 
• 18185-81-4 (E)-oct-3-en-1-ol 
• 57491-33-5 E-11-Hexadecenal 
• 61301-56-2 trans-11-hexadecen-1-ol 
• 2277-16-9 (E)-non-4-enal 
• 16695-34-4 (E)-4-none-1-ol 
• 53042-79-8 1-acetoxyhexadeca-7Z,11E-diene 
• 2132-80-1 4,4'-Dimethoxybiphenyl 
• 423765-09-7 E-1-methoxy-4-(3'-octenyl)benzene 
• 132255-29-9 8-phenylsulfonyl-11E-hexadecen-1-ol 
• 51812-91-0 1-(2-tetrahydropyranyloxy)-9E-tetradecene 
• 35329-50-1 (E)-4-nonenoic acid 

Relevant articles and documents

Chain-modified pyridino-N substituted nicotine compounds for use in the treatment of CNS pathologies

Compounds for treating abuse of nicotinic receptor agonists, addiction to psychostimulant drugs, addiction to opiates, addiction to alcohol, addiction to tobacco products, addiction to nicotine, schizophrenia and related diseases, depression and related conditions, Alzheimer's disease, Parkinson's disease, irritable bowel syndrome, and colitis. The compounds competitively inhibit central nervous system acting nicotinic receptor agonists and act at the putative α3β2* and α4β2 neuronal nicotinic receptors in the central nervous system.

Regiospecific Nucleophilic Substitution in Cyclopropylcarbinols. Stereospecific Opening of the Cyclopropane Ring

Reactions of cyclopropylcarbinols with hydrobromic acid and the triphenylphosphine-tetrabromomethane complex at 0°C result in stereospecific opening of the cyclopropane ring with formation of trans-homoallyl bromides.

SIMPLE SYNTHESIS OF ACETOGENIN TRANSOID INSECT PHEROMONES STARTING FROM ACETYLCYCLOPROPANE

A highly effective synthesis of a series of alkyl and 1-alkenyl cyclopropyl ketones, which are key components in the complete synthesis of a large number of transoid lepidoptera pheromones, has been developed, based on the alkylation of N-cyclohexyl-1-cyclopropylethylideneimine or its condensation with aldehydes.