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13857-03-9

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13857-03-9 Usage

General Description

Z-7-Decen-1-yl Acetate is a chemical compound that is used as a pheromone in many types of insects, particularly moths and butterflies. The compound has the ability to attract these insects, which makes it useful in both agricultural settings, for pest control purposes, and in scientific research to study insect behavior. It is classified as an Alkenyl compound and is also known as Dec-7-enyl Acetate. Despite its potent activity towards insects, it's generally considered safe for humans and the environment, assuming it's used properly. The chemical structure consists of a decenyl group (10-carbon alkene group) attached to an acetate group.

Check Digit Verification of cas no

The CAS Registry Mumber 13857-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13857-03:
(7*1)+(6*3)+(5*8)+(4*5)+(3*7)+(2*0)+(1*3)=109
109 % 10 = 9
So 13857-03-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-3-4-5-6-7-8-9-10-11-14-12(2)13/h4-5H,3,6-11H2,1-2H3/b5-4-

13857-03-9SDS

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 dec-7-enyl acetate

1.2 Other means of identification

Product number -
Other names 7Z-decen-1-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:13857-03-9 SDS

13857-03-9Downstream Products

13857-03-9Relevant articles and documents

Short and stereoselective syntheses of pheromone components of Aproaerema modicella

Yadav,Chandrasekhar,Kache

, p. 4035 - 4043 (1995)

Efficient syntheses of pheromone components of Aproaerema modicella starting from a common intermediate 7-octyn-1-ol is described.

Exo- and Endohormones. XI. Synthesis of Monounsaturated Sex Pheromones of Lepitoptera via α-Dicetones

Oprean, I.,Ciupe, Hilke,Gansca, Lucia,Hodosan, F.

, p. 283 - 289 (2007/10/02)

α-Dicetones (5), prepared starting either with cyanohydrines (1) or with N,N-diethyl oxamate (6), were converted via the dihydrazones 11 ito acetylenes (12).Replacement of the protecting group by the acatate group and partial stereoselective reduction of the triple bond led finally to the title conpounds.

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