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109-68-2

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109-68-2 Usage

Chemical Properties

colourless liquid

Uses

2-Pentene (mixture of cis and trans) is used in the synthesis of polycyclopentene by ring-opening metathesis polymerization.

General Description

2-Pentene undergoes addition reaction with phenoxathiin cation radical in acetonitrile solution to form bis(10-phenoxathiiniumyl)alkane adducts.

Purification Methods

Reflux the mixture with sodium wire, then fractionally distil it twice through a Fenske (glass helices packing, p 11) column. [Beilstein 1 IV 815.]

Check Digit Verification of cas no

The CAS Registry Mumber 109-68-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109-68:
(5*1)+(4*0)+(3*9)+(2*6)+(1*8)=52
52 % 10 = 2
So 109-68-2 is a valid CAS Registry Number.
InChI:InChI=1/2C5H10/c2*1-3-5-4-2/h2*3,5H,4H2,1-2H3/b5-3+;5-3-

109-68-2 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (A17736)  2-Pentene, cis + trans, 98%   

  • 109-68-2

  • 25g

  • 767.0CNY

  • Detail
  • Alfa Aesar

  • (A17736)  2-Pentene, cis + trans, 98%   

  • 109-68-2

  • 100g

  • 2290.0CNY

  • Detail

109-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name sym-Methylethylethylene

1.2 Other means of identification

Product number -
Other names 2-Pentene,c

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:109-68-2 SDS

109-68-2Related news

High-pressure X-ray photoelectron spectroscopy of palladium model hydrogenation catalysts. Part 2: Hydrogenation of TRANS-2-PENTENE (cas 109-68-2) on palladium08/19/2019

We have performed the first “high-pressure” X-ray photoelectron spectroscopy (XPS) study on the palladium, hydrogen, and olefin (trans-2-pentene) system to gain better insight into the hydrogenation reaction. We report here data collected with the use of a Pd(111) single crystal and a polycrys...detailed

109-68-2Relevant articles and documents

Feit et al.

, p. 2799 (1973)

-

Lewis,Coppinger

, p. 796,797 (1954)

-

-

Boozer,Lewis

, p. 3182 (1953)

-

Catalytic dehydrogenation of alcohol over solid-state molybdenum sulfide clusters with an octahedral metal framework

Kamiguchi, Satoshi,Okumura, Kazu,Nagashima, Sayoko,Chihara, Teiji

, p. 188 - 190 (2015)

Abstract Solid-state molybdenum sulfide clusters with an octahedral metal framework, the superconducting Chevrel phases, are applied to catalysis. A copper salt of a nonstoichiometric sulfur-deficient cluster, CuxMo6S8-δ (x = 2.94 and δ ≈ 0.3), is stored in air for more than 90 days. When the oxygenated cluster is thermally activated in a hydrogen stream above 300 °C, catalytic activity for the dehydrogenation of primary alcohols to aldehydes and secondary alcohols to ketones develops. The addition of pyridine or benzoic acid decreases the dehydrogenation activity, indicating that both a Lewis-acidic coordinatively unsaturated molybdenum atom and a basic sulfur ligand synergistically act as the catalytic active sites.

-

Lewis,Pearce

, p. 2039,2040 (1964)

-

Reactions of Sodium Diisopropylamide: Liquid-Phase and Solid-Liquid Phase-Transfer Catalysis by N, N, N′, N″, N″-Pentamethyldiethylenetriamine

Algera, Russell F.,Collum, David B.,Ma, Yun,Woltornist, Ryan A.

, p. 13370 - 13381 (2021)

Sodium diisopropylamide (NaDA) in N,N-dimethylethylamine (DMEA) and DMEA-hydrocarbon mixtures with added N,N,N′,N″,N″-pentamethyldiethylenetriamine (PMDTA) reacts with alkyl halides, epoxides, hydrazones, arenes, alkenes, and allyl ethers. Comparisons of PMDTA with N,N,N′,N′-tetramethylethylenediamine (TMEDA) accompanied by detailed rate and computational studies reveal the importance of the trifunctionality and κ2-κ3 hemilability. Rate studies show exclusively monomer-based reactions of 2-bromooctane, cyclooctene oxide, and dimethylresorcinol. Catalysis with 10 mol % PMDTA shows up to >30-fold accelerations (kcat > 300) with no evidence of inhibition over 10 turnovers. Solid-liquid phase-transfer catalysis (SLPTC) is explored as a means to optimize the catalysis as well as explore the merits of heterogeneous reaction conditions.

Constructing PtI?COF for semi-hydrogenation reactions of phenylacetylene

Li, Jian Hong,Yu, Zhi Wu,Li, Jian Qiang,Fan, Ya Ling,Gao, Zhi,Xiong, Jian Bo,Wang, Li,Tao, Yuan,Yang, Li Xiao,Xiao, Yu Xin,Luo, Feng

, (2020)

The great efforts have been devoted to fabricate excellent hydrogenation catalysts owing to the broad applications in industrial fields. However, the preparation processes of traditional hydrogenation catalysts are often complicated. Herein, mono-valence PtI?COF was synthesized as a catalyst for semi-hydrogenation of phenylacetylene for the first time. The easily prepared SO3H-linked COF possesses a two-dimensional eclipsed layered-sheet structure, making its incorporation with metal ions feasible. The as-prepared PtI?COF composite exhibits excellent performance for semi-hydrogenation phenylacetylene with 93.5% conversion and 90.2% selectivity to styrene under mild reaction conditions (1 ?bar H2, 25 ?°C) within 20 ?min. It's worth noting that the turnover frequency (TOF) value reaches at 3965 h-1, which outperforms most of recently reported excellent Pt-based catalysts for this reaction.

CATALYST SYSTEMS THAT INCLUDE METAL OXIDE CO-CATALYSTS FOR THE PRODUCTION OF PROPYLENE

-

Paragraph 0069-0070, (2020/05/02)

Embodiments of methods of synthesizing a metathesis catalyst system, which include impregnating tungsten oxide on silica support in the presence of a precursor to produce a base catalyst; calcining the base catalyst; impregnating a metal oxide co-catalyst comprising a metal oxide onto the surface of the base catalyst to produce a doped catalyst; and calcining the doped catalyst to produce a metathesis catalyst system. Further embodiments of processes for the production of propylene, which include contacting a hydrocarbon feedstock comprising a mixture of 1-butene and 2-butene with embodiments of the metathesis catalyst system to produce, via metathesis conversion, a product stream comprising propylene.

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