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14919-01-8

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14919-01-8 Usage

General Description

Trans-3-octene is a colorless liquid hydrocarbon with the molecular formula C8H16. It is an organic compound classified as an alkene and is commonly used as a building block and intermediate in the production of various chemicals, such as plastics, synthetic lubricants, and fragrances. Its chemical structure consists of a chain of eight carbon atoms with a double bond between the third and fourth carbon atoms. Trans-3-octene is primarily produced through the catalytic dehydrogenation of octane or by the metathesis reaction of butene. It is known for its mild, sweet odor and is considered to be relatively stable under normal conditions. However, it may react vigorously with strong oxidizing agents and is incompatible with strong acids and bases. Its main applications include its use as a monomer in the production of polyethylene, which is used in various plastic products, and as a component in the synthesis of specialized organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 14919-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,1 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14919-01:
(7*1)+(6*4)+(5*9)+(4*1)+(3*9)+(2*0)+(1*1)=108
108 % 10 = 8
So 14919-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-3-5-7-8-6-4-2/h5,7H,3-4,6,8H2,1-2H3

14919-01-8 Well-known Company Product Price

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  • Alfa Aesar

  • (43154)  trans-3-Octene, 97%   

  • 14919-01-8

  • 2g

  • 274.0CNY

  • Detail
  • Alfa Aesar

  • (43154)  trans-3-Octene, 97%   

  • 14919-01-8

  • 10g

  • 1203.0CNY

  • Detail
  • Alfa Aesar

  • (43154)  trans-3-Octene, 97%   

  • 14919-01-8

  • 50g

  • 5445.0CNY

  • Detail

14919-01-8SDS

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 trans-3-Octene

1.2 Other means of identification

Product number -
Other names TRANS-3-OCTENE

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:14919-01-8 SDS

14919-01-8Relevant articles and documents

Kinetics of the Sodium-Ammonia Reduction of 3-Octyne

Dewald, Robert R.,Ekstein, Cynthia J.,Song, Woo M.

, p. 6921 - 6922 (1987)

The reduction of 3-octyne by sodium in liquid ammonia was studied kinetically with use of conventional conductometric techniques.The reaction was found to obey the second-order differential rate law-dam->/dt=2kam->.An activation energy of 3.8 +/- 0.9 kcal/mol was calculated.The presence of a weak acid (H2O) markedly increased the reaction rate.A mechanism in which protonation of the radical anion is the rate-determining step is suggested.

Continuous flow hydrogenation with Pd complexes of pyridine-benzotriazole ligands

Y?lmaz, Filiz,Hür, Deniz

, (2021/08/03)

The use of continuous flow systems in chemical synthesis provides great advantages in terms of sustainability, efficiency, and safety. The ability to control reaction parameters such as temperature, pressure, and catalyst exposure in flow system enables rapid optimization of reaction conditions. In the present study, palladium complexes of 1-(piridin-2-il)-1H-benzo[d][1,2,3]triazol, N-((1H-benzo[d][1,2,3]triazol-1-il)metil)piridin-2-amin, and (1H-benzo[d][1,2,3]triazol-1-yl)(pyridin-2-yl)methanone ligands were synthesized and characterized. The catalytic activities of complexes are investigated in the hydrogenation of various alkenes such as styrene, cyclohexene, and 1-octene under continuous flow conditions. The complexes showed very high activity at 10-bar H2 pressure and 50°C for short periods of 5–10?min. The catalysts reused for 10 cycles with no significant loss of catalytic activity.

Ni-Catalyzed Isomerization-Hydrocyanation Tandem Reactions: Access to Linear Nitriles from Aliphatic Internal Olefins

Gao, Jihui,Ni, Jie,Yu, Rongrong,Cheng, Gui-Juan,Fang, Xianjie

supporting information, p. 486 - 490 (2021/02/05)

A highly regioselective nickel-based catalyst system for the isomerization/hydrocyanation of aliphatic internal olefins is described. This benign tandem reaction provides facile access to a wide variety of aliphatic nitriles in good yields with excellent regioselectivities. Thanks to Lewis acid-free conditions, the protocol features board functional groups tolerance, including secondary amine and unprotected alcohol groups.

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