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1,3,6-Octatriene is an organic compound with the molecular formula C8H12, consisting of an eight-carbon chain with three carbon-carbon double bonds located at the 1st, 3rd, and 6th positions. It is a conjugated diene, meaning the double bonds are separated by a single bond, which results in unique chemical properties and reactivity. This colorless liquid is insoluble in water but soluble in organic solvents. 1,3,6-Octatriene is synthesized through various methods, such as the Diels-Alder reaction, and is used in the production of polymers, pharmaceuticals, and other chemical compounds. It is also known for its potential applications in materials science and as a precursor in the synthesis of more complex organic molecules.

929-20-4

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929-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929-20-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 929-20:
(5*9)+(4*2)+(3*9)+(2*2)+(1*0)=84
84 % 10 = 4
So 929-20-4 is a valid CAS Registry Number.

929-20-4Downstream Products

929-20-4Relevant academic research and scientific papers

Imidazolium salts and the use of these ionic liquids as a solvent and as a catalyst

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Example 6, (2008/06/13)

New 1,2,3- or 1,2,3,4- or 1,2,3,4,5- substituted imidazolium salts and their uses as solvent in catalyzed organic reactions, as well as compositions containing them and a transition metal compound. They can be used in the following reactions : the telomerisation of conjugated dienes, the dimerisation of olefins, the oligomerisation of olefins, the polymerization of olefins, the alkylation of olefins, the hydrogenation of olefins, the olefin metathesis, the hydroformylation of olefins, the ring-closing metathesis of olefins, the ring-opening metathesis polymerisation of olefins, the symetric or asymetric epoxidation of olefins (including heteroatom substituted olefins) and the cyclopropanation of olefins, the condensation reaction, the hydrogenation reaction, the isomerization reaction, the Suzuki cross-coupling reactions, the amination reaction, the partial oxidation of alkancs, the kinetic resolution of racemic mixtures, the hydrogenation of imines, the hydrogenation of ketones, the transfer hydrogenation and the hydroxylation of aromatic organic compounds.

SYNTHESE DE LIGANDS DE TYPE AMINO-DIPHOSPHINITES; ETUDE EN RMN 13 C ET 31 P. APPLICATION A LA DIMERISATION DU BUTADIENE PAR LES COMPLEXES DU NICKEL

Bendayan, Andree,Masotti, Henriette,Peiffer, Gilbert,Siv, Chhan,Faure, Robert

, p. 289 - 298 (2007/10/02)

The new chiral aminodiphosphinite ligands are readily prepared from chiral amino acids.These compounds were characterized by 13 C and 31 P NMR spectroscopy and their behaviour as homogeneous catalysts was investigated in the linear dimerization of butadiene.

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