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104410-91-5

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104410-91-5 Usage

Description

NONACOSADIENE (7Z,11Z), also known as 7(Z),11(Z)-Nonacosadiene, is an unsaturated cuticular hydrocarbon that functions as a pheromone in insects, specifically in the Drosophila melanogaster species, commonly known as fruit flies. This C29 diene is sexually dimorphic, meaning it occurs and has effects differently in males and females. In female fruit flies, it acts as a cuticular pheromone that stimulates male courtship behavior. The biosynthesis of NONACOSADIENE (7Z,11Z) is believed to be mediated by an elongase enzyme, which has female-based expression.

Uses

Used in Chemical Communication Research:
NONACOSADIENE (7Z,11Z) is used as a subject of study in chemical communication research for understanding the role of pheromones in insect behavior, particularly in the courtship behavior of male fruit flies. The research on this pheromone can provide insights into the chemical signals and their impact on mating and reproductive success in insects.
Used in Insect Attractant Development:
NONACOSADIENE (7Z,11Z) is used as a key component in the development of insect attractants, specifically for fruit flies. By mimicking the natural pheromone, these attractants can be employed in pest control strategies to lure and trap male fruit flies, thereby disrupting their mating patterns and reducing their population.
Used in Pheromone-based Pest Control:
In the agricultural industry, NONACOSADIENE (7Z,11Z) is used as a pheromone in pest control strategies to manage fruit fly populations. By incorporating this pheromone into traps or other control methods, it is possible to reduce the number of fruit flies that damage crops and spread diseases, ultimately protecting the agricultural yield and reducing the need for chemical pesticides.
Used in Behavioral Ecology Studies:
In the field of behavioral ecology, NONACOSADIENE (7Z,11Z) is used as a model compound to study the evolution of sexual dimorphism and the role of chemical signals in mating systems. Understanding the function and evolution of this pheromone can provide valuable information on the mechanisms driving sexual selection and the development of mating preferences in insects.

Check Digit Verification of cas no

The CAS Registry Mumber 104410-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,1 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104410-91:
(8*1)+(7*0)+(6*4)+(5*4)+(4*1)+(3*0)+(2*9)+(1*1)=75
75 % 10 = 5
So 104410-91-5 is a valid CAS Registry Number.

104410-91-5SDS

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 7(Z),11(Z)-Nonacosadiene

1.2 Other means of identification

Product number -
Other names -

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:104410-91-5 SDS

104410-91-5Downstream Products

104410-91-5Relevant articles and documents

Ti-catalyzed cross-cyclomagnesiation of 1,2-dienes in the stereoselective synthesis of insect pheromones

D'yakonov, Vladimir A.,Islamov, Ilgiz I.,Makarov, Aleksey A.,Dzhemilev, Usein M.

, p. 1755 - 1757 (2017)

The Ti-catalyzed intermolecular cross-cyclomagnesiation reaction of aliphatic and oxygenated 1,2-dienes with Grignard reagents was used as the key step to develop facile stereoselective methods for preparation of the major components of citrus leafminer moth (Phyllocnistis citrella) pheromones as well as cotton pink bollworm (Pectinophora gossypiella) and fruit fly (Drosophila melanogaster) attractants.

Synthesis of 7,11-dienes from enol ether and Grignard reagents under nickel catalysis: sex pheromones of Drosophila melanogaster

Davis,Carlson

, p. 936 - 938 (2007/10/02)

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