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3-Methyl-trans-2-hexene is an organic compound with the molecular formula C7H14. It is a colorless liquid with a strong, pungent odor. This unsaturated hydrocarbon belongs to the class of alkenes, specifically a mono-olefin, and features a carbon-carbon double bond between the second and third carbon atoms. The presence of a methyl group (CH3) attached to the third carbon atom distinguishes it from other hexene isomers. 3-Methyl-trans-2-hexene is used as a chemical intermediate in the synthesis of various organic compounds, such as fragrances, pharmaceuticals, and polymers. It is also found in trace amounts in some essential oils and natural products. Due to its reactive nature, it is sensitive to air, light, and heat, and should be stored under controlled conditions to maintain its stability and purity.

20710-38-7

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20710-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20710-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,1 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20710-38:
(7*2)+(6*0)+(5*7)+(4*1)+(3*0)+(2*3)+(1*8)=67
67 % 10 = 7
So 20710-38-7 is a valid CAS Registry Number.

20710-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-methylhex-2-ene

1.2 Other means of identification

Product number -
Other names 3-METHYL-2-HEXENE

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:20710-38-7 SDS

20710-38-7Relevant academic research and scientific papers

Silica-supported dendrimer-palladium complex-catalyzed selective hydrogenation of dienes to monoolefins

Zweni, Pumza P.,Alper, Howard

, p. 725 - 731 (2007/10/03)

The selective hydrogenation of cyclic and acyclic dienes to monoolefins occurs under very mild conditions, in the presence of silica-supported PAMAM-Pd complexes. The activity and selectivity of this reaction is sensitive to the dendrimer structure. These dendritic complexes display excellent recycle properties, retaining activity for up to eight recycles.

CYCLIZATION OF C7-ALKANES OVER Pt BLACK CATALYST

Zimmer, H.,Paal, Z.,Tetenyi, P.

, p. 513 - 532 (2007/10/02)

C6-and C5-cyclization of heptane isomers (and also, olefin formation as a related process) over Pt-black have been studied in pulse and circulation systems.Hydrogendeficient conditions favour aromatization, via presumably terminal olefins.C5-Cyclization in the presence of more hydrogen is accompanied by internal olefin formation.Relative reactivities of all heptane isomers have been measured; this shows that cyclization is easier between terminal methyl groups.Optimum hydrogen pressures for both types of cyclization have been determined (and compared with hydrogenolysis, too).Earlier mechanism suggestion for aromatization and cyclopentane formation have been confirmed; the distinction between two types of bond shift mechanisms producing aromatics (from substituted pentanes) and saturated isomers, respectively, has recieved additional support facilitating the identification of these two reactions with mechanisms proposed in the literature.

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