174064-00-7

Usage

Uses

Used in Organic Synthesis:
7-TETRADECYN-6,9-DIOL is utilized as a reactant in the production of a wide range of compounds, including pharmaceuticals, agrochemicals, and polymers. Its presence in organic synthesis is attributed to its ability to participate in various chemical reactions, contributing to the creation of diverse products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 7-TETRADECYN-6,9-DIOL is used as a building block for the synthesis of medicinal compounds. Its unique structure allows it to be incorporated into the development of new drugs, potentially leading to advancements in medicine.
Used in Agrochemical Industry:
7-TETRADECYN-6,9-DIOL is employed as a reactant in the synthesis of agrochemicals, such as pesticides and herbicides. Its role in this industry is to contribute to the development of more effective and environmentally friendly agricultural products.
Used in Materials Science:
In the field of materials science, 7-TETRADECYN-6,9-DIOL is used as a component in the development of new materials with specific properties. Its unique structure and reactivity make it a valuable asset in creating innovative materials for various applications.

Upstream product

• 629-05-0 n-octyne 
• 66-25-1 hexanal 
• 818-72-4 1-Octyn-3-ol 
• 183428-36-6 tetradec-7-yne-6-ol 

Relevant academic research and scientific papers

[3,3]-Sigmatropic Rearrangements in the Enantioselective Synthesis of (-)-Methylenolactocin

A Pd(II)-catalyzed [3,3]-sigmatropic rearrangement is used to transfer chirality from an enantio-enriched alk-3-ene-1,2-diol to a C2- symmetrical alk-2-ene-1,4-diol which, in turn, can be converted into a precursor of (-)-methylenolactocin through an additional [3,3]-sigmatropic rearrangement (either Johnson orthoester or Ireland-Claisen rearrangement).

A concise synthesis of (-)-methylenolactocin and (-)- phaseolinic acid from (6S,9S)-tetradec-7-yne-6,9-diol

A novel, stereodivergent route to paraconic acids from C2-symmetric trans- and cis-alk-2-ene-1,4-diols through Ireland-Claisen and/or Johnson orthoester rearrangements is disclosed. This strategy has been applied to the synthesis of (-)-methylenolactocin and (-)-phaseolinic acid from a single chiral diol.

Unsaturated syn - And anti -1,2-amino alcohols by cyclization of allylic bis-trichloroacetimidates. Stereoselectivity dependence on substrate configuration

Disubstituted allylic bis-imidates undergo Lewis acid catalyzed or spontaneous cyclization to oxazolines, which are precursors of unsaturated amino alcohols. Stereoselectivity of the cyclization is mainly determined by the substrate configuration. Highly