TRANS-2-OCTENE

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TRANS-2-OCTENE

  • Name TRANS-2-OCTENE
  • CAS 13389-42-9
  • Purity 99%
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Product Details

Cost-effective customized wholesale TRANS-2-OCTENE 13389-42-9

  • Molecular Formula: C8H16
  • Molecular Weight: 112.215
  • Vapor Pressure: 31 mm Hg ( 37.7 °C) 
  • Melting Point: -89--86°C 
  • Refractive Index: n20/D 1.413(lit.) 
  • Boiling Point: 123 °C(lit.)
     
  • Flash Point: 21.1°C 
  • PSA: 0.00000 
  • Density: 0.727g/cm3 
  • LogP: 3.14280 

TRANS-2-OCTENE(Cas 13389-42-9) Usage

Purification Methods

Purify it as for 1-octene above. [Beilstein 1 IV 879.]

General Description

trans-2-Octene undergoes epoxidation with two manganese(III) porphyrin complexes by meta-chloroperbenzoic acid under catalytic reaction conditions in various solvents.

InChI:InChI=1/C8H16/c1-3-5-7-8-6-4-2/h5,7H,3-4,6,8H2,1-2H3/b7-5+

13389-42-9 Relevant articles

Facile access to tuneable Schwartz's reagents: Oxidative addition products from the reaction of amide N-H bonds with reduced zirconocene complexes

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On the tracks of Schwartz's reagent: Two...

Cluster versus non-cluster catalysis in olefin thermal isomerization and hydrosilylation in the presence of Ru(CO)12

Hilal, Hikmat S.,Khalaf, Shukri,Jondi, Waheed

, p. 167 - 173 (1993)

The ruthenium cluster Ru3(CO)12 (1) has ...

Catalytic isomerization and disproportionation of olefins promoted by group 4/d0 benzamidinate complexes

Averbuj, Claudia,Eisen, Moris S.

, p. 8755 - 8759 (1999)

The group 4/d0 benzamidinate complexes c...

Reactivity of osmium-rhodium mixed-metal cluster [Os3Rh(μ-H)3(CO)12] towards vinyl containing ligands

Po-Kwan Lau, Jasmine,Wong, Wing-Tak

, p. 151 - 158 (2002)

Reaction of [Os3Rh(μ-H)3(CO)12] (1) with...

Highly Z-Selective Double Bond Transposition in Simple Alkenes and Allylarenes through a Spin-Accelerated Allyl Mechanism

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Double-bond transposition in alkenes (is...

Designing and synthesis of phosphine derivatives of Ru3(CO)12 – Studies on catalytic isomerization of 1-alkenes

Pandya, Chayan,Panicker, Rakesh R.,Senjaliya, Parth,Hareendran, M.K. Hima,Anju,Sarkar, Sibasis,Bhat, Haamid,Jha, Prakash C.,Rao, Koya Prabhakara,Smith, Gregory S.,Sivaramakrishna, Akella

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A comparative investigation on the isome...

Extension of surface organometallic chemistry to metal?organic frameworks: Development of a well-defined single site [(≡Zr? O?)W(=O)(CH2TBu)3] olefin metathesis catalyst

Thiam, Zeynabou,Abou-Hamad, Edy,Dereli, Busra,Liu, Lingmei,Emwas, Abdul-Hamid,Ahmad, Rafia,Jiang, Hao,Isah, Abdulrahman Adamu,Ndiaye, Papa Birame,Taoufik, Mostafa,Han, Yu,Cavallo, Luigi,Basset, Jean-Marie,Eddaoudi, Mohamed

, p. 16690 - 16703 (2020)

We report here the first step by step an...

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Van Ende,D.,Krief,A.

, p. 2709 - 2712 (1975)

-

Convenient Stereoselective Synthesis of the Three Isomeric 2,6-Octadienes

Walba, David M.,Wand, Michael D.,Wilkes, Martin C.

, p. 2259 - 2261 (1980)

-

Gold(I)-mediated hydrothiolation of conjugated olefins

Brouwer, Chad,Rahaman, Ronald,He, Chuan

, p. 1785 - 1789 (2007)

Thiol additions to conjugated olefins we...

Nonredox Metal-Ion-Accelerated Olefin Isomerization by Palladium(II) Catalysts: Density Functional Theory (DFT) Calculations Supporting the Experimental Data

Senan, Ahmed M.,Qin, Shuhao,Zhang, Sicheng,Lou, Chenling,Chen, Zhuqi,Liao, Rong-Zhen,Yin, Guochuan

, p. 4144 - 4148 (2016)

Redox metal-ion-catalyzed olefin isomeri...

Effect of Carboxylate Ligands on Alkane Dehydrogenation with (dmPhebox)Ir Complexes

Yuan, Hongmei,Brennessel, William W.,Jones, William D.

, p. 2326 - 2329 (2018)

A series of carboxylate-ligated iridium ...

SYNTHESES A L'ACIDE DE SULFONES (XXIV).SYNZHESE STEREOSELECTIVE D'OLEFINES PAR HYDROGENOLISE DES VINYLSULFONES.

Bremner, John,Julia, Marc,Launay, Michele

, p. 3265 - 3266 (1982)

The now readily available E or Z vivylsu...

Formation and reactivity of a Co4-μ-alkyne cluster from a Co(I)-alkene complex

Weding, Nico,Spannenberg, Anke,Jackstell, Ralf,Hapke, Marko

, p. 5660 - 5663 (2012)

Highly reactive Co(I) complex [CpCo(H2C=...

Metal-catalyzed chemical activation of calcium carbide: New way to hierarchical metal/alloy-on-carbon catalysts

Ananikov, Valentine P.,Lebedev, Andrey N.,Mironenko, Roman M.,Rodygin, Konstantin S.,Saybulina, Elina R.

, p. 281 - 289 (2022/02/23)

A simple and efficient strategy for the ...

Ruthenium-Catalyzed E-Selective Partial Hydrogenation of Alkynes under Transfer-Hydrogenation Conditions using Paraformaldehyde as Hydrogen Source

Fetzer, Marcus N. A.,Tavakoli, Ghazal,Klein, Axel,Prechtl, Martin H. G.

, p. 1317 - 1325 (2021/02/11)

E-alkenes were synthesized with up to 10...

Method for synthesizing alkyl olefin through coupling of double-bond carbon-hydrogen bond and saturated carbon-hydrogen bond

-

Paragraph 0060-0064; 0089, (2021/02/10)

The invention discloses a method for syn...

Method for synthesizing 1, 2-disubstituted olefin through reaction of terminal group olefin and sulfoxide

-

Paragraph 0053-0054; 0057-0062; 0076, (2021/02/10)

The invention discloses a method for syn...

13389-42-9 Process route

methyl radical
2229-07-4

methyl radical

isopropyl radical
2025-55-0

isopropyl radical

t-Butyl radical
1605-73-8

t-Butyl radical

1-bromo-octane
111-83-1

1-bromo-octane

octane
111-65-9

octane

cis-2-octene
7642-04-8

cis-2-octene

trans-2-Octene
13389-42-9

trans-2-Octene

oct-1-ene
111-66-0,25068-25-1

oct-1-ene

Conditions
Conditions Yield
oct-2-yne
2809-67-8

oct-2-yne

trans-2-Octene
13389-42-9

trans-2-Octene

Conditions
Conditions Yield
With formaldehyd; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; water; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In toluene; at 80 ℃; for 2h; stereoselective reaction;
53%
With ammonia; sodium;

13389-42-9 Upstream products

  • 2229-07-4
    2229-07-4

    methyl radical

  • 2025-55-0
    2025-55-0

    isopropyl radical

  • 1605-73-8
    1605-73-8

    t-Butyl radical

  • 111-83-1
    111-83-1

    1-bromo-octane

13389-42-9 Downstream products

  • 58567-47-8
    58567-47-8

    (2E)-1N-(p-toluenesulfonamido)-octene

  • 58567-46-7
    58567-46-7

    4-Tosylamino-trans-2-octen

  • 101161-20-0
    101161-20-0

    (4-Methyl-5-pentyl-2-phenyl-isoxazolidin-3-yl)-phenyl-methanone

  • 101161-21-1
    101161-21-1

    (5-Methyl-4-pentyl-2-phenyl-isoxazolidin-3-yl)-phenyl-methanone

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