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6108-62-9

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6108-62-9 Usage

Description

(5Z,7Z)-dodeca-5,7-diene is a hydrocarbon compound belonging to the class of alkenes, which are organic compounds containing carbon-carbon double bonds. With the chemical formula C12H22, this compound consists of a chain of 12 carbon atoms and 22 hydrogen atoms. The "5Z,7Z" designation indicates the specific arrangement of the double bonds in the molecule.

Uses

Used in Organic Synthesis:
(5Z,7Z)-dodeca-5,7-diene is used as a building block in organic synthesis for its ability to undergo various chemical reactions, such as addition reactions and polymerization. Its unique structure allows for the creation of a wide range of compounds with different properties and applications.
Used in Fragrance and Flavor Industry:
(5Z,7Z)-dodeca-5,7-diene is used as a raw material in the production of fragrances and flavoring agents. The characteristic double bond structure of this compound imparts specific odors and tastes to the end products, making it valuable in the creation of scents and flavors for various consumer products.
Used in Material Development:
(5Z,7Z)-dodeca-5,7-diene may be used as a component in the development of new materials, potentially contributing to the creation of innovative products with unique properties.
Used in Pharmaceutical Research:
(5Z,7Z)-dodeca-5,7-diene may have potential applications in the pharmaceutical industry, where its unique structure could be leveraged in the design and synthesis of new drugs.
Used in Agrochemicals:
(5Z,7Z)-dodeca-5,7-diene could also be utilized in the development of new agrochemicals, such as pesticides or herbicides, where its chemical properties may provide novel modes of action or increased efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 6108-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6108-62:
(6*6)+(5*1)+(4*0)+(3*8)+(2*6)+(1*2)=79
79 % 10 = 9
So 6108-62-9 is a valid CAS Registry Number.

6108-62-9SDS

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 (5Z,7Z)-dodeca-5,7-diene

1.2 Other means of identification

Product number -
Other names cis,cis-1,4-Di-n-butyl-1,3-butadiene

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:6108-62-9 SDS

6108-62-9Downstream Products

6108-62-9Relevant articles and documents

A frustrated-Lewis-pair approach to catalytic reduction of alkynes to cis-alkenes

Chernichenko, Konstantin,Madarasz, Adam,Papai, Imre,Nieger, Martin,Leskelae, Markku,Repo, Timo

, p. 718 - 723 (2013/08/23)

Frustrated Lewis pairs are compounds containing both Lewis acidic and Lewis basic moieties, where the formation of an adduct is prevented by steric hindrance. They are therefore highly reactive, and have been shown to be capable of heterolysis of molecular hydrogen, a property that has led to their use in hydrogenation reactions of polarized multiple bonds. Here, we describe a general approach to the hydrogenation of alkynes to cis-alkenes under mild conditions using the unique ansa-aminohydroborane as a catalyst. Our approach combines several reactions as the elementary steps of the catalytic cycle: hydroboration (substrate binding), heterolytic hydrogen splitting (typical frustrated-Lewis-pair reactivity) and facile intramolecular protodeborylation (product release). The mechanism is verified by experimental and computational studies.

Configurational Instability of α-Alkenyl and α-Alkynyl Vinyllithiums. Syntheses of Stereodefined 2-Alkyl-1-en-3-ynes

Miller, Joseph A.,Leong, William,Zweifel, George

, p. 1839 - 1840 (2007/10/02)

Metal-halogen exchange of either (Z)-enynyl bromides or (Z)-dienyl bromides by sec-BuLi produces vinyllithiums that are configurationally stable only at temperatures below -120 deg C and -78 deg C, respectively.Allylation of (Z)-enynylalanates with allyl bromide or methylation of (Z)-enynyl bromides with CH3MgI and Fe(acac)3 catalyst furnishes the corresponding 2-alkyl-1-en-3-ynes.

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