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Trans-2-methyl-3-hexene is an organic compound with the molecular formula C7H14. It is a colorless, flammable liquid that belongs to the class of alkenes, specifically a mono-olefin. This chemical is characterized by a double bond between the second and third carbon atoms in a six-carbon chain, with a methyl group attached to the second carbon. It is an isomer of 2-methyl-3-hexene, differing in the position of the double bond. Trans-2-methyl-3-hexene is used as a chemical intermediate in the synthesis of various compounds, such as fragrances, pharmaceuticals, and polymers. It is also found in trace amounts in some essential oils and can be used as a solvent. Due to its reactive nature, it should be handled with care, following proper safety protocols.

3899-36-3

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3899-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3899-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3899-36:
(6*3)+(5*8)+(4*9)+(3*9)+(2*3)+(1*6)=133
133 % 10 = 3
So 3899-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H14/c1-4-6-7(3)5-2/h6H,4-5H2,1-3H3/b7-6+

3899-36-3SDS

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 (E)-3-methylhex-3-ene

1.2 Other means of identification

Product number -
Other names trans-3-Methyl-3-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:3899-36-3 SDS

3899-36-3Downstream Products

3899-36-3Relevant academic research and scientific papers

High yield of liquid range olefins obtained by converting i-propanol over zeolite H-ZSM-5

Mentzel, Uffe V.,Shunmugavel, Saravanamurugan,Hruby, Sarah L.,Christensen, Claus H.,Holm, Martin S.

experimental part, p. 17009 - 17013 (2010/03/23)

Methanol, ethanol, and i-propanol were converted under methanol-to-gasoline (MTH)-like conditions (400°C, 1-20 bar) over zeolite H-ZSM-5. For methanol and ethanol, the catalyst lifetimes and conversion capacities are comparable, but when i-propanol is use

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.

Stereoselective synthesis of vicinal dilithioalkenes by addition of lithium metal, to carbon-carbon triple bonds

Maercker,Girreser

, p. 8019 - 8034 (2007/10/02)

The reaction of various cyclic and acyclic alkynes with lithium dust (2% sodium) to form vicinal dilithioalkenes has been investigated. Aliphatic alkynes, e.g. 3-hexyne (27a), exclusively afford the corresponding (E)-dilithioalkenes, insoluble solids which are stable at room temperature and allow access to a variety of tetrasubstituted olefins in acceptable yields.

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