1002-33-1

Basic information

• Product Name: 1,3-OCTADIENE
• Synonyms: 1,3-OCTADIENE;(3E)-1,3-Octadiene;1,3-OCTADIENE 98%;(E)-1,3-Octadiene
• CAS NO: 1002-33-1
• Molecular Formula: C₈H₁₄
• Molecular Weight: 110.2
• Mol File: 1002-33-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 130-131℃
• Flash Point: 17.2±13.0℃
• Appearance: /
• Density: 0.738±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 13.4mmHg at 25°C
• Refractive Index: 1.4501 (589.3 nm 20℃)
• CAS DataBase Reference: 1,3-OCTADIENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-OCTADIENE(1002-33-1)
• EPA Substance Registry System: 1,3-OCTADIENE(1002-33-1)

Safety Data

• Hazardous Substances Data: 1002-33-1(Hazardous Substances Data)

Usage

General Description

1,3-Octadiene is a colorless, flammable liquid with a strong, unpleasant odor. It is a chemical compound with the formula C8H14 and is classified as an alpha-omega diene. 1,3-Octadiene is primarily used in the production of synthetic rubber, as it can be polymerized to form elastomers with properties similar to natural rubber. It is also used as a monomer in the production of plastics and resins. Additionally, 1,3-Octadiene is used in the synthesis of various organic compounds and as a solvent in industrial processes. However, it is considered hazardous and should be handled with care due to its flammability and potential health risks if inhaled or ingested.

InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h3,5,7H,1,4,6,8H2,2H3

Upstream product

• 3391-86-4 1-octen-3-ol 
• 104-88-1 4-chlorobenzaldehyde 
• 74-85-1 ethene 
• 106-99-0 buta-1,3-diene 
• 25152-84-5 trans,trans-2,4-decadienal 
• 152212-49-2 1,2-dibromooctane 
• 2442-10-6 oct-1-en-3-yl acetate 
• 122-52-1 triethyl phosphite 

Downstream Products

• 106-79-6 dimethyl sebacate 
• 109-43-3 dibutyl sebacate 
• 111-65-9 octane 

Relevant articles and documents

Synthesis and pyrolysis of two flavor precursors of oct-1-en-3-yl methylpyrazinecarboxylates

To rich flavor additive species of pyrazines, two new compounds of 3,6-dimethyl-2,5-pyrazinedicarboxylic acid 1-octen-3-yl ester (DMPOE) and 3,5,6-trimethyl-2-pyrazinecarboxylic acid 1-octen-3-yl ester (TMPOE) were synthesized by KMnO4 oxidatio

Palladium-catalyzed preparation of dialkyl allylphosphonates. A new preparation of diethyl 2-oxoethylphosphonate

Palladium-catalyzed Michaelis-Arbuzov reaction of allyl acetates with trialkyl phosphites affords dialkyl allylphosphonates. Diethyl 2-oxoethylphosphonate is efficiently prepared by ozonization of diethyl allylphosphonate.

METAL COMPLEXES IN ORGANIC SYNTHESIS. VIII. ALLYLIC ALCOHOLS AS STARTING MATERIALS IN PALLADIUM-CATALYZED WITTIG-TYPE OLEFINIZATIONS.

Allylic alcohols, aldehydes, and triphenylphosphine participate in a one-pot process catalyzed by palladium, which is formally equivalent to the Wittig olefinization. It can be applied to both aliphatic and aromatic aldehydes. The resulting olefins which appear as mixtures of stereoisomers were fully hydrogenated. Two different mechanisms can account for the observed results.