19093-20-0

Basic information

• Product Name: (E)-oct-5-en-2-one
• Synonyms: (E)-oct-5-en-2-one;(E)-5-Octen-2-one;5-Octen-2-one, (5E)-;5-Octen-2-one, (E)-;Einecs 242-810-9
• CAS NO: 19093-20-0
• Molecular Formula: C₈H₁₄O
• Molecular Weight: 126.19616
• EINECS: 242-810-9
• Mol File: 19093-20-0.mol

Chemical Properties

• Boiling Point: 174.4°Cat760mmHg
• Flash Point: 52.1°C
• Appearance: /
• Density: 0.833g/cm³
• Vapor Pressure: 1.21mmHg at 25°C
• Refractive Index: 1.431
• CAS DataBase Reference: (E)-oct-5-en-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-oct-5-en-2-one(19093-20-0)
• EPA Substance Registry System: (E)-oct-5-en-2-one(19093-20-0)

Safety Data

• Hazardous Substances Data: 19093-20-0(Hazardous Substances Data)

Usage

Uses

Used in the Food Industry:
(E)-oct-5-en-2-one is used as a flavoring agent for its fruity, mushroom-like odor, adding a unique and appealing taste to various food products.
Used in the Fragrance Industry:
(E)-oct-5-en-2-one is used as a fragrance ingredient in perfumes and personal care products, leveraging its pleasant aroma to enhance the scent profiles of these products.
Used in the Production of Polymers:
(E)-oct-5-en-2-one serves as a valuable component in the production of polymers, contributing to the development of various materials with diverse applications.
Used in Organic Synthesis:
As a precursor in organic synthesis, (E)-oct-5-en-2-one plays a crucial role in the creation of other chemical compounds, further expanding its utility in the chemical industry.

InChI:InChI=1/C8H14O/c1-3-4-5-6-7-8(2)9/h4-5H,3,6-7H2,1-2H3/b5-4+

Upstream product

• 7348-71-2 (E)-1-bromo-2-pentene 
• 1007476-32-5 sodium ethyl acetylacetate enolate 
• 20036-40-2 1-(2-vinyl-cyclopropyl)-ethanone 
• 917-54-4 methyllithium 
• 109-67-1 1-penten 
• 78-95-5 chloroacetone 
• 616-25-1 1-Penten-3-ol 
• 116-11-0 2-Methoxypropene 

Downstream Products

• 108012-80-2 oct-5t-en-2-one-(2,4-dinitro-phenylhydrazone) 

Relevant articles and documents

UNIQUE HALOGEN-INDUCED CYCLIZATIONS, REAGENTS THEREFOR, AND COMPOUNDS PRODUCED THEREBY

This disclosure is related to halonium compounds useful for cyclization of polyenes, alkenoic acids, and alkenyl alkyl ethers, and halogenation of aromatic compounds. The synthesis of such halonium compounds, compounds made using such halonium compounds, and synthesis of natural compounds, including decalins, using the halonium compounds is also disclosed. A representative halonium compound of the disclosure is: Formula (I).

A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia -type bromoethers

A unique procedure to effect a ring-expanding bromoetherification process is described, wherein tetrahydrofurans and tetrahydropyrans are smoothly transformed into 8- and 9-membered bromoethers in a regio- and stereocontrolled manner through the use of BDSB (bromodiethylsulfonium bromopentachloroantimonate). These products resemble the cores of the Laurencia C15 acetogenins. In light of the generality and effectiveness of the approach, this work provides a unique strategy for their laboratory preparation and may implicate a possible biosynthesis pathway.

Lewis Acid-Induced Reactions of γ-Trialkylstannyl Ketones. Cyclization, Carbon-Carbon Bond Cleavage, and 1,5-Hydride Shift

γ-Trialkylstannyl ketones underwent cyclobutanation, C-C bond cleavage, or 1,5-hydride shift, depending upon the substitution pattern of the substrates.