Production Method 1

111-70-6

616-12-6

141-93-5

931-88-4

575-37-1

2146-37-4

930-18-7

690-08-4

19037-72-0

624-64-6

52161-57-6

16327-38-1

824-90-8

622-96-8

264-09-5

3404-65-7

691-38-3

824-22-6

14686-13-6

2808-79-9

Reaction Conditions

1.1 Catalysts: Vanadium ;  100 - 550 °C

Reference

Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

, World Intellectual Property Organization, , ,

2-Pentene, 3-methyl-,(2E)- Raw materials

• 1-Heptanol

2-Pentene, 3-methyl-,(2E)- Preparation Products

• 1,3-DIETHYLBENZENE (141-93-5)
• Cyclooctene (931-88-4)
• 1,7-Dimethylnaphthalene (575-37-1)
• Ethylidenecyclopentane (2146-37-4)
• Cyclopropane,1,2-dimethyl-, (1R,2S)-rel- (930-18-7)
• 2-Pentene,4,4-dimethyl-, (2E)- (690-08-4)
• Cyclopentene,4,4-dimethyl- (19037-72-0)
• 2-BUTENE (624-64-6)
• Benzene, 1-methyl-3-(1-methyl-2-propenyl)- (52161-57-6)
• Cyclobutene, 3,3-dimethyl- (16327-38-1)
• Benzene, 1-buten-1-yl- (824-90-8)
• 4-Ethyltoluene (622-96-8)
• 7H-Benzocycloheptene (264-09-5)
• 3-methyl-3-hexene (c,t) (3404-65-7)
• 2-Pentene, 3-methyl-,(2E)- (616-12-6)
• cis-4-Methyl-2-pentene (691-38-3)
• 4-Methylindan (824-22-6)
• 2-Heptene, (2E)- (14686-13-6)
• Cyclohexene,1,4-dimethyl- (2808-79-9)

• 1. Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe?
  Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
• 2. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 3. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 4. Enantio- & chemo-selective preparation of enantiomerically enriched aliphatic nitro alcohols using Candida parapsilosis ATCC 7330
  Sowmyalakshmi Venkataraman RSC Adv., 2015,5, 73807-73813
• 5. Dissociation of large gaseous serine clusters produces abundant protonated serine octamer
  Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625

• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Unsaturated hydrocarbons Branched unsaturated hydrocarbons
• Solvents and Organic Chemicals Organic Compounds Acids/Esters
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Comprehensive Guide to 2-Pentene, 3-methyl-, (2E)- (CAS No. 616-12-6): Properties, Applications, and Market Insights

2-Pentene, 3-methyl-, (2E)-, also known as (2E)-3-Methyl-2-pentene, is an important organic compound with the CAS number 616-12-6. This unsaturated hydrocarbon belongs to the class of alkenes and is widely used in various industrial and research applications. Its unique chemical structure and properties make it a valuable component in organic synthesis, flavor and fragrance production, and polymer chemistry.

The molecular formula of 2-Pentene, 3-methyl-, (2E)- is C₆H₁₂, and it features a double bond at the 2-position with a methyl group at the 3-position. The (2E) designation indicates the trans-configuration of the substituents around the double bond, which significantly influences its chemical reactivity and physical properties. This compound is a colorless liquid at room temperature with a characteristic hydrocarbon odor, and it is soluble in most organic solvents but insoluble in water.

One of the most significant applications of 2-Pentene, 3-methyl-, (2E)- is in the field of organic synthesis. It serves as a versatile building block for the preparation of more complex molecules. Researchers and chemists value this compound for its ability to participate in various addition reactions, polymerization processes, and catalytic transformations. The double bond in its structure makes it particularly useful for creating fine chemicals and specialty materials.

In the flavor and fragrance industry, 2-Pentene, 3-methyl-, (2E)- finds application as an intermediate for synthesizing aroma compounds. Its hydrocarbon skeleton can be modified to produce various terpenes and terpenoids, which are essential components in many natural and synthetic fragrances. The compound's structural features contribute to the creation of green, woody, and fruity notes in perfumery.

The polymer industry also benefits from 2-Pentene, 3-methyl-, (2E)- as it can act as a comonomer in certain polyolefin production processes. When incorporated into polymer chains, it can influence the material's crystallinity, flexibility, and thermal properties. This makes it valuable for developing specialized plastics and elastomers with tailored characteristics for specific applications.

Recent advancements in green chemistry have brought attention to compounds like 2-Pentene, 3-methyl-, (2E)- as potential bio-based intermediates. With growing interest in sustainable chemical processes, researchers are exploring ways to derive such molecules from renewable resources rather than traditional petroleum sources. This aligns with current market trends favoring environmentally friendly production methods.

From a market perspective, the demand for 2-Pentene, 3-methyl-, (2E)- has shown steady growth, particularly in regions with strong chemical manufacturing sectors. The Asia-Pacific market, in particular, has seen increased consumption due to expanding pharmaceutical and specialty chemical industries. Global suppliers are focusing on improving production efficiency and purity standards to meet the evolving needs of various industries.

Quality control is crucial when working with 2-Pentene, 3-methyl-, (2E)-. Standard analytical techniques such as gas chromatography (GC) and nuclear magnetic resonance (NMR) spectroscopy are typically employed to verify its purity and identity. The compound is generally stable under recommended storage conditions but should be kept away from strong oxidizers and ignition sources.

Researchers interested in 2-Pentene, 3-methyl-, (2E)- often search for information about its spectral data, synthetic applications, and safety handling procedures. Recent publications have explored its use in catalytic asymmetric synthesis and as a model compound for studying olefin metathesis reactions. These studies contribute to the growing body of knowledge about this versatile chemical intermediate.

For laboratory use, 2-Pentene, 3-methyl-, (2E)- is typically available through chemical suppliers in various quantities and purity grades. When purchasing, it's important to consider factors such as package size, storage requirements, and technical support availability. Many suppliers now provide detailed technical data sheets and certificates of analysis to ensure customers have complete information about the product.

As the chemical industry continues to evolve, compounds like 2-Pentene, 3-methyl-, (2E)- will likely find new applications in emerging fields such as advanced materials and renewable energy technologies. Its combination of structural simplicity and chemical versatility makes it an interesting subject for ongoing research and development efforts across multiple scientific disciplines.

• 52428-73-6(1,5-Octadiene, 6-methyl-)
• 19780-67-7(2-Pentene,3-ethyl-2-methyl-)
• 10574-37-5(2,3-Dimethyl-2-pentene)
• 4914-89-0(3-Hexene, 3-methyl-,(3Z)-)
• 16789-51-8(3-Ethyl-3-hexene)
• 19550-88-0(3-Hexene,3,4-dimethyl-, (3E)-)
• 3899-36-3(3-Hexene, 3-methyl-,(3E)-)
• 30951-95-2(3-Hexene, 3,4-dimethyl-)
• 19550-87-9(3-Hexene,3,4-dimethyl-, (3Z)-)
• 51886-28-3(Heptane, 3-methyl-,didehydro deriv. (9CI))