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16725-53-4

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16725-53-4 Usage

Chemical Properties

clear colorless liquid

Uses

(Z)-9-Tetradecenyl Acetate is one of the sex pheromone components of Ostrinia genus in Japan.

Hazard

Low toxicity by ingestion.

Check Digit Verification of cas no

The CAS Registry Mumber 16725-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16725-53:
(7*1)+(6*6)+(5*7)+(4*2)+(3*5)+(2*5)+(1*3)=114
114 % 10 = 4
So 16725-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h6-7H,3-5,8-15H2,1-2H3/b7-6-

16725-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-tetradec-9-enyl] acetate

1.2 Other means of identification

Product number -
Other names cis-9-Tetradecenyl acetate

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:16725-53-4 SDS

16725-53-4Relevant articles and documents

SYNTHESIS OF ONE OF THE SEX PHEROMONES OF Heliothis levre - cis-TETRADEC-9-EN-1-OL ACETATE

Dzhumakulov, T.,Yuldashev, A. M.,Abduvakhabov, A. A.

, p. 516 - 517 (1982)

-

Polymer-anchored Organosilyl Protecting Group in Organic Synthesis

Chan, Tak-Hang,Huang, Wen-Qiang

, p. 909 - 911 (1985)

Polymer-anchored dimethyl- and diphenyl-chlorosilanes (1a) and (1b) have been prepared and polymer (1b) was found to be useful for the protection of the hydroxy functional group; its use in the synthesis of an insect sex pheromone is reported.

SYNTHESIS OF DEC-5Z-ENYL ACETATE AND TETRADEC-9Z-ENYL ACETATE - COMPONENTS OF THE SEX PHEROMONE OF Agrotis segetum

Verba, G. G.,Bikulova, L. M.,Abduvakhabod, A. A.

, p. 130 - 131 (1988)

-

SYNTHESIS OF PHEROMONE DERIVATIVES VIA Z-SELECTIVE OLEFIN METATHESIS

-

Paragraph 0261-0262, (2021/12/28)

Disclosed herein are methods for synthesizing fatty olefin metathesis products of high Z-isomeric purity from olefin feedstocks of low Z-isomeric purity. The methods include contacting a contacting an olefin metathesis reaction partner, such as acylated alkenol or an alkenal acetal, with an internal olefin in the presence of a Z-selective metathesis catalyst to form the fatty olefin metathesis product. In various embodiments, the fatty olefin metathesis products are insect pheromones. Pheromone compositions and methods of using them are also described.

PRODUCTION OF FATTY OLEFIN DERIVATIVES VIA OLEFIN METATHESIS

-

, (2017/06/12)

In one aspect, the invention provides a method for synthesizing a fatty olefin derivative. The method includes: a) contacting an olefin according to Formula I with a metathesis reaction partner according to Formula IIb in the presence of a metathesis catalyst under conditions sufficient to form a metathesis product according to Formula IIIb: and b) converting the metathesis product to the fatty olefin derivative. Each R1 is independently selected from H, C1-18 alkyl, and C2-18 alkenyl; R2b is C1-8 alkyl; subscript y is an integer ranging from 0 to 17; and subscript z is an integer ranging from 0 to 17. In certain embodiments, the metathesis catalyst is a tungsten catalyst or a molybdenum catalyst. In various embodiments, the fatty olefin derivative is a pheromone. Pheromone compositions and methods of using them are also described.

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