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10,12-Hexadecadien-1-ol, (Z,Z)- is a naturally occurring organic compound, specifically a polyunsaturated alcohol, characterized by the presence of two double bonds in its structure. It is commonly found in various plant species and is known for its distinct floral scent. 10,12-Hexadecadien-1-ol, (Z,Z)- is used in the fragrance industry to create natural, fresh, and green notes in perfumes and other scented products. Its chemical formula is C16H30O, and it is also referred to as (Z,Z)-10,12-hexadecadien-1-ol or (Z,Z)-6,9-hexadecadien-1-ol. The (Z,Z) notation indicates the configuration of the double bonds, which are in the cis configuration, meaning that the hydrogen atoms are on the same side of the double bond. This configuration plays a role in the compound's aroma and reactivity.

765-18-4

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765-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 765-18-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 765-18:
(5*7)+(4*6)+(3*5)+(2*1)+(1*8)=84
84 % 10 = 4
So 765-18-4 is a valid CAS Registry Number.

765-18-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (10Z,12Z)-hexadeca-10,12-dien-1-ol

1.2 Other means of identification

Product number -
Other names (10Z,12Z)-hexadecadien-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:765-18-4 SDS

765-18-4Relevant academic research and scientific papers

Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones

De Figueiredo, Renata Marcia,Berner, Raphael,Julis, Jennifer,Liu, Ting,Tuerp, David,Christmann, Mathias

, p. 640 - 642 (2007/10/03)

Shuffling of two simple building blocks and a regioselective transfer hydrogenation allow for the rapid synthesis of a small collection of lepidopteran sex pheromones, e.g., 8E,10Z-tetradeca-8,10-dienal 5c, from the horse chestnut leafminer (Cameraria ohridella).

Synthesis of (E,E)-10,12-hexadecadienal and (Z)-11-octadecenal

Yadav, J. S.,Balakrishnan, Kamalam,Sivadasan, Latha

, p. 297 - 302 (2007/10/02)

Two economically important insect pheromones, viz. (E,E)-10,12-hexadecadien-1-al (1) and (Z)-11-octadecenal (2) of cotton pests have been synthesised from cheap and readily available materials utilising in situ alkylation of dianion of 4-pentyn-1-ol obtainable easily by lithium amide induced opening of tetrahydrofurfuryl chloride in liquid ammonia.

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