42134-50-9

Usage

Uses

Used in Chemical Production:
2,3-EPOXYOCTANAL is used as a precursor in the synthesis of various chemicals, primarily for the production of polymers and resins. Its unique chemical structure makes it a valuable component in the creation of these materials, which are utilized in a wide range of industries.
Used in Perfumery and Fragrance Industry:
Leveraging its strong odor, 2,3-EPOXYOCTANAL is employed as a raw material in the synthesis of perfumes and fragrances. Its distinctive scent profile contributes to the development of complex and appealing fragrances for various consumer products.
Used in Environmental and Health Risk Assessment:
Given its irritant effects and potential environmental hazard, 2,3-EPOXYOCTANAL is also used in the context of environmental and health risk assessments. These assessments are crucial for understanding and managing the potential impacts of this chemical on human health and the environment, ensuring safe handling and usage protocols are in place.

Upstream product

• 2548-87-0 (E)-2-Octenal 
• 101758-85-4 2,3-epoxyoctanol 
• 629-05-0 n-octyne 
• 20052-00-0 1,1-Diethoxy 2(E)-octene 
• 33861-21-1 2-bromo-1,1-diethoxyoctane 
• 35066-22-9 2-bromooctanal 
• 124-13-0 Octanal 
• 18409-17-1 (E)-oct-2-en-1-ol 

Downstream Products

• 75899-68-2 (E)-4-Hydroxy-2-nonenal 
• 586963-15-7 1-[3-(2-deoxy-5-(4,4'-dimethoxytrityl)-β-D-erythro-pentofuranosyl)-3H-imidazo[2,1-i]purin-7-yl]-1-hexyl-2-methylpropanoate 

Relevant academic research and scientific papers

Microwave-assisted synthesis of N -isobutyl-4,5-epoxy-2(E)-decenamide

A new and efficient synthesis of a naturally occurring amide alkaloid, N-isobutyl-4,5-epoxy-2(E)-decenamide isolated from the roots of Piper nigrum has been described involving a total of nine steps. Octanal and 2-bromoacetic acid have been used as the starting materials.

Oxidation catalysis of Nb(salan) complexes: Asymmetric epoxidation of allylic alcohols using aqueous hydrogen peroxide as an oxidant

Several optically active Nb(salan) complexes were synthesized, and their oxidation catalysis was examined. A dimeric μ-oxo Nb(salan) complex that was prepared from Nb(OiPr)5 and a salan ligand was found to catalyze the asymmetric epoxidation of allylic alcohols using a urea-hydrogen peroxide adduct as an oxidant with good enantioselectivity. However, subsequent studies of the time course of this epoxidation and of the relationship between the ee of the ligand and the ee of the product indicated that the μ-oxo dimer dissociates into a monomeric species prior to epoxidation. Moreover, monomeric Nb(salan) complexes prepared in situ from Nb(OiPr)5 and salan ligands followed by water treatment were found to catalyze the epoxidation of allylic alcohols better using aqueous hydrogen peroxide in CHCl3/brine or toluene/brine solution with high enantioselectivity ranging from 83 to 95% ee, except for the reaction of cinnamyl alcohol that showed a moderate ee of 74%. This is the first example of the highly enantioselective epoxidation of allylic alcohols using aqueous hydrogen peroxide as an oxidant.

Site-specific incorporation of the 1-hexanol-1,N6-etheno-2′-deoxyadenosine adduct into oligodeoxyribonucleotides

Modified oligonucleotides that contain the hydrophobic 1-hexanol-1,N6-etheno-2′-deoxyadenosine adduct have been synthesized using a mild solid phase phosphoramidite chemistry. The presence and the integrity of the modified nucleoside in the syn

Polymer supported perruthenate (PSP): Clean oxidation of primary alcohols to carbonyl compounds using oxygen as cooxidant

Molecular oxygen has been used as stoichiometric oxidant in polymer supported perruthenate (PSP) catalysed conversion of primary alcohols to carbonyl compounds affording pure products without the need for conventional workup procedures.

Polymer Supported Perruthenate (PSP): A new oxidant for clean organic synthesis

A polymer supported perruthenate reagent has been prepared and used in the conversion of primary and secondary alcohols to aldehydes and ketones, respectively, affording pure products without the need for conventional work-up procedures.

Diastereoselective addition reactions of allylstannanes to carbonyl groups in the side-chain of π-allyltricarbonyliron lactone complexes

Lewis acid-mediated addition of allylstannanes to ketones adjacent to the allyl system of π-allyltricarbonyliron lactone complexes generates the corresponding homoallylic tertiary alcohols with excellent diastereocontrol.

CYCLODEXTRIN-H2O2: A NEW SYSTEM FOR ASYMMETRIC EPOXIDATION

Asymmetric epoxidation of trans-cinnamaldehyde and chalcone by the use of H2O2 as an oxidizing agent in alkaline media in the presence of cyclodextrins gave the corresponding epoxides with enantiomeric excess up to 8percent.