73010-83-0

Usage

Chemical classification

Long-chain unsaturated alcohol

Structure

17-carbon chain with a double bond at the 10th position

Designation

(10Z)indicating the position and configuration of the double bond

Natural occurrence

Found in nature, particularly in various insect species

Biological role

Acts as a pheromone, especially as a sex attractant for certain moth species

Synthetic applications

Used in the production of fragrance compounds

Synthesis utility

Serves as a building block in the synthesis of other organic molecules

Potential applications

Agriculture, pest control, and pharmaceutical research due to effects on insect behavior and communication

Molecular weight

Approximately 258.45 g/mol
These properties and contents provide a comprehensive overview of 10-Heptadecen-1-ol, (10Z)-, highlighting its structure, natural occurrence, and potential applications in various fields.

Upstream product

• 151329-53-2 Heptadec-10-yn-1-ol 
• 55695-90-4 2-(9-bromononyloxy)tetrahydropyran 
• 629-05-0 n-octyne 
• 177903-00-3 2-Heptadec-10-ynyloxy-tetrahydro-pyran 

Downstream Products

• 162250-89-7 (Z)-1-Brom-10-heptadecen 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of (+)-docosa-4,15-dien-l-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure, and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations

The (4E,15Z)-, and (4￡,15￡)-isomers of (+)-docosa-4,15-dien-l-yn-3-ol 1, isolated from the marine sponge Cribroclialina vasculwn, were synthesized in highly enantiomerically pure form by lipase-mediated biotransformation with Novozym 435, and the structur

Synthesis of Natural Compounds with Alkyl-methoxy-1,4-benzoquinone Structure

The 1,4-benzoquinones 1-7 occurring in various plants and having interesting biological properties have been synthesized from the tetrahydropyranyl ethers 17 and 21.Reaction with n-butyllithium gave selectively the ortho-lithiated compounds.These could be alkylated with the haloalkenes 13-16 and haloalkanes to give the substituted phenols 18-20 and 22-25 in high yield after methanolysis.Alkylations of the methoxyisopropylether 8 of 10-undecyn-1-ol with bromobutane and bromohexane gave 9 and 10.These alkynols could be selectively hydrogenated with Lindlar-Palladium catalyst to give the (Z)-alkenols 11 and 12 which could be converted into the bromoalkenes 13, 14 and the iodoalkenes 15, 16.Oxidation of the phenols 18-20 and 22-25 with molecular oxygen in the presence of salcomine as catalyst produced the substituted 1,4-benzoquinones 1-3 and 26-29 in high yield.Selective hydrolysis with perchloric acid converted 26-29 into the natural products 4-7. - Key Words: Tetrahydropyranyl-ethers / ortho-Lithiation / ortho-Alkylation / 1,4-Benzoquinones, alkyl-methoxy- / 1,4-Benzoquinones, alkyl-hydroxy-methoxy-