2768-12-9

Usage

Uses

Used in Fragrance Industry:
2,6-Dimethylheptan-1-ol is used as a fragrance ingredient for its floral, fruity scent, adding depth and complexity to perfumes and personal care products.
Used in Pharmaceutical Industry:
2,6-Dimethylheptan-1-ol is used as an active ingredient in the development of antifungal medications, leveraging its antifungal properties to combat fungal infections.
Used in Solvent Applications:
2,6-dimethylheptan-1-ol is utilized as a solvent in various applications, including the dissolution of other substances and participation in chemical reactions.
Used in Chemical Synthesis:
2,6-Dimethylheptan-1-ol serves as a chemical intermediate in the production of other compounds, playing a crucial role in the synthesis of a range of chemical products.

InChI:InChI=1/C9H20O/c1-8(2)5-4-6-9(3)7-10/h8-10H,4-7H2,1-3H3

Upstream product

• 84606-47-3 ammonium 2,6-dimethylheptyl sulfate 
• 3327-66-0 2,6-dimethylheptanal 
• 106-72-9 2,6-dimethyl-5-hepten-1-al 

Relevant academic research and scientific papers

Isolation and absolute configuration determination of aliphatic sulfates as the Daphnia kairomones inducing morphological defense of a phytoplankton

2,6-Dimethylheptyl sulfate (1) and 6-methyloctyl sulfate (3) were isolated from Daphnia pulex as the Daphnia kairomones that induced morphological defense of a freshwater phytoplankton Scenedesmus gutwinskii var. heterospina (NIES-802). The absolute stere

METHOD FOR PRODUCING UNSATURATED ALCOHOL

PROBLEM TO BE SOLVED: To provide a method for producing an unsaturated alcohol that uses an unsaturated carbonyl compound as a raw material and can produce an unsaturated alcohol in which only the carbonyl bond of the unsaturated carbonyl compound is selectively reduced with excellent reaction rate, high selectivity and high yield. SOLUTION: The process for producing an unsaturated alcohol includes a step of allowing the reductive reaction of a 3C or more unsaturated carbonyl compound having one or more carbon-carbon unsaturated bonds in the molecule with hydrogen to proceed in the presence of a catalyst comprising at least one kind of metal selected from the group consisting of cobalt, nickel, copper, zinc, ruthenium, rhodium, palladium, silver, osmium, iridium and platinum and at least one kind of metal selected from the group consisting of vanadium, chromium, manganese, iron, molybdenum, tungsten and rhenium to produce a corresponding unsaturated alcohol. COPYRIGHT: (C)2015,JPOandINPIT

Rapid synthesis of unsaturated alcohols under mild conditions by highly selective hydrogenation

Ir-ReOx/SiO2 acted as a highly active and selective heterogeneous catalyst for the hydrogenation of unsaturated aldehydes to unsaturated alcohols in water at low H2 pressure (0.8 MPa) and low temperature (303 K). The catalysis is derived from the synergy between Ir metal and ReOx.

Triflimide-catalysed sigmatropic rearrangement of N-allylhydrazones as an example of a traceless bond construction

The recognition of structural elements (that is, retrons) that signal the application of specific chemical transformations is a key cognitive event in the design of synthetic routes to complex molecules. Reactions that produce compounds without an easily identifiable retron, by way of either substantial structural rearrangement or loss of the atoms required for the reaction to proceed, are significantly more difficult to apply during retrosynthetic planning, yet allow for non-traditional pathways that may facilitate efficient acquisition of the target molecule. We have developed a triflimide (Tf 2 NH)-catalysed rearrangement of N-allylhydrazones that allows for the generation of a sigma bond between two unfunctionalized sp 3 carbons in such a way that no clear retron for the reaction remains. This new traceless bond construction displays a broad substrate profile and should open avenues for synthesizing complex molecules using non-traditional disconnections.