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11-cis Vaccenyl Acetate is a male-specific mating pheromone of the fruit fly D. melanogaster, which plays a crucial role in orchestrating the mating and social behaviors of insects. It selectively acts through the Or67d odorant receptor to control mating behavior in both male and female fruit flies.
Used in Insect Control:
11-cis Vaccenyl Acetate is used as a pheromone in insect control for attracting and trapping male fruit flies, helping to manage and control their population.
Used in Chemical Ecology Research:
11-cis Vaccenyl Acetate is used as a research tool in chemical ecology to study the mechanisms of insect mating and social behaviors, as well as the role of pheromones in these processes.
Used in Pheromone-based Pest Management:
11-cis Vaccenyl Acetate is used in pheromone-based pest management strategies to disrupt the mating behavior of fruit flies, reducing their population and protecting crops from damage.
Used in Insect Attractants:
11-cis Vaccenyl Acetate is used as an insect attractant in various applications, such as monitoring insect populations, studying insect behavior, and developing new pest control methods.

6186-98-7

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6186-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6186-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6186-98:
(6*6)+(5*1)+(4*8)+(3*6)+(2*9)+(1*8)=117
117 % 10 = 7
So 6186-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h8-9H,3-7,10-19H2,1-2H3/b9-8-

6186-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-cis Vaccenyl Acetate

1.2 Other means of identification

Product number -
Other names Methylol methyl hexyl ketone 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:6186-98-7 SDS

6186-98-7Relevant academic research and scientific papers

INSECT PHEROMONES AND THEIR ANALOGS III. SYNTHESIS OF THE SEX ATTRACTANTS OF SOME LEPIDOPTERA

Dzhemilev, U. M.,Balezina, G. G.,Volkova, L. A.,Krivonogov, V. P.,Tolstikov, G. A.

, p. 82 - 85 (2007/10/02)

A new route to the synthesis of a number of attractants of Lepidoptera (Argyrotaenia velutinana, Mamestra configurata, and Lycorea ceres ceres) have been developed.These substances are acetates of enols with the cis configuration: tetradec-11-en-1-ol, hexadec-11-en-1-ol, and octadec-11-en-1-ol, respectively.The constants of the substances obtained agree completely with those given in the literature.The method is based on the coupling of the C3, C5, and C7 aldehydes with methyl 11-bromoundecanoate (I) by the Wittig reaction.To obtain compound (I) from methyl undeca-2E,5E,10-trienoate or methyl undeca-10-enoate we used hydroboration according to Brown followed by hydrogenation and bromination of the alcohol obtained.The advantage of this method is the use as starting materials of esters of unsaturated acids readily obtained by the homogeneous catalytic co-oligomerization of 1,3-dienes with acrylates.

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