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(E)-4-Dodecene, also known as trans-4-Dodecene, is an organic compound with the molecular formula C12H24. It is a colorless liquid with a strong, pungent odor and is classified as an alkene due to the presence of a carbon-carbon double bond. This unsaturated hydrocarbon is a member of the dodecenes family and is characterized by its linear structure with a double bond located at the 4th carbon atom. (E)-4-Dodecene is used as a chemical intermediate in the synthesis of various compounds, such as fragrances, lubricants, and plasticizers. It is also employed in the production of specialty chemicals and pharmaceuticals. Due to its reactivity, it is essential to handle (E)-4-Dodecene with care, as it can undergo addition reactions with various reagents, making it a versatile building block in organic chemistry.

7206-15-7

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7206-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7206-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7206-15:
(6*7)+(5*2)+(4*0)+(3*6)+(2*1)+(1*5)=77
77 % 10 = 7
So 7206-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H24/c1-3-5-7-9-11-12-10-8-6-4-2/h7,9H,3-6,8,10-12H2,1-2H3/b9-7+

7206-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-dodecene

1.2 Other means of identification

Product number -
Other names 4-dodecene

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:7206-15-7 SDS

7206-15-7Downstream Products

7206-15-7Relevant academic research and scientific papers

Asymmetric allylic alkylation of acyclic allylic ethers with organolithium reagents

Pérez, Manuel,Fa?anás-Mastral, Martín,Hornillos, Valentín,Rudolph, Alena,Bos, Pieter H.,Harutyunyan, Syuzanna R.,Feringa, Ben L.

supporting information, p. 11880 - 11883 (2012/10/29)

A highly efficient, regio- and enantioselective CuI/ phosphoramidite-catalyzed asymmetric allylic alkylation of allyl ethers with organolithium reagents is reported (see scheme). The use of organolithium reagents is essential for this catalytic C-C bond formation due to their compatibility with different Lewis acids. The versatility of allylic ethers under the copper-catalyzed reaction conditions with organolithium reagents is demonstrated in the shortest synthesis of (S)-Arundic acid. Copyright

Reduction of acetylenic compounds to (E)-olefins by alkali metals - An investigation of the scope

Brandsma, Lambert,Nieuwenhuizen, Willem F.,Zwikker, Jan W.,Maeeorg, Uno

, p. 775 - 779 (2007/10/03)

Efficient procedures have been developed for the stereospecific reduction by alkali metals of disubstituted acetylenes with long carbon chains. Acetylenes containing two or more (isolated) triple bonds are reduced considerably more easily than are monoyne

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