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(3E,6E)-1,3,6-Octatriene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22038-69-3

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22038-69-3 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 97, p. 341, 1975 DOI: 10.1021/ja00835a019

Check Digit Verification of cas no

The CAS Registry Mumber 22038-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,3 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22038-69:
(7*2)+(6*2)+(5*0)+(4*3)+(3*8)+(2*6)+(1*9)=83
83 % 10 = 3
So 22038-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-3-5-7-8-6-4-2/h3-7H,1,8H2,2H3/b6-4+,7-5+

22038-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E,6E)-octa-1,3,6-triene

1.2 Other means of identification

Product number -
Other names (3E,6E)-1,3,6-Octatriene

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:22038-69-3 SDS

22038-69-3Downstream Products

22038-69-3Relevant academic research and scientific papers

Nickel(0) and palladium(0) complexes with 1,3,5-triaza-7-phosphaadamantane. Catalysis of buta-1,3-diene oligomerization or telomerization in an aqueous biphasic system

Cermak, Jan,Kvicalova, Magdalena,Blechta, Vratislav

, p. 355 - 363 (2007/10/03)

New homoleptic nickel(0) and palladium(0) complexes with a water-soluble ligand, 1,3,5-triaza-7-phosphaadamantane, were prepared and characterized by 1H, 13C, and 31P NMR spectra. The complexes, together with the known ana

Interaction of vinylpyridines with 1,3-dienes catalyzed by transition metal complexes

Selimov, F. A.,Ptashko, O. A.,Fatykhov, A. A.,Khalikova, N. R.,Dzhemilev, U. M.

, p. 872 - 878 (2007/10/02)

The linear and cyclic cooligomerization of 2-vinyl-, 2-methyl-5-vinyl-, and 4-vinylpyridines with 1,3-dienes and trienes catalyzed by complexes of transition metals (Fe, Co, Ni, Mn, Cr, Pd, Ru, Rh, and Zr) was carried out to give unsaturated pyridines containing alkenyl and cycloalkenyl substituents.

DIMERISATION DE DIENES CONJUGUES A L'AIDE DE COMPLEXES DU NICKEL EN PRESENCE DE LIGANDS DE TYPE AMINOPHOSPHINITE ETUDE D'OPTIMISATION

Masotti, Henriette,Pfeiffer, Gilbert,Siv, Chhan,Courbis, Pierre,Sergent, Michelle,Phan TAN LUU, Roger

, p. 63 - 77 (2007/10/02)

New chiral aminophosphinite ligands are readily prepared and their behaviour as homogeneous catalysts was investigated in the linear dimerization of butadiene and isoprene.This latter reaction has been optimised using experimental research methodology, leading to a conversion rate above 50percent.

Change of Selectivity in Catalytic Multicomponent Systems via Concentrations, Control of Metal-Catalyzed Reactions, Part XIII

Bartik, Tamas,Behler, Ansgar,Heimbach, Paul,Ndalut, Paulo,Sebastian, Joerg,Sturm, Harald

, p. 1529 - 1535 (2007/10/02)

By applying the method of inverse titration the influence of increasing concentrations of added effectors to organic and metalorganic chemical systems on the product selectivity can easily be identified.To a Wittig-type system we added LiI (change of stereoselectivity) and also triphenylphosphanoxide (removal of salt-effect).To a catalytic Ni(0)/butadiene system we added triphenylphosphite and then morpholine and vice versa.Ni:P(OC6H5)3:morpholine in a ratio 1:1:0.1 yields more than 90percent cyclodimers but in a ratio 1:0.1:20 more than 90percent n-octa-1,3,6-trienes.The co- oligomerisation of two butadienes with one 2,5-dimethyl-3-aza-hex-3-en in the system Ni/triphenylphosphane/butadiene/Schiff base/toluene/effector (1:1:66:33:66: ca. 0.1) leads - within the 2:1-cooligomers - by adding di-n-propyl-borane to a pure octadienylated Schiff base 11 or by adding morpholine largely to an octatrienylated amine 12 (ca. 85percent 12 and ca. 15percent 11). - Key words: Inverse Titration, Wittig Reactions, Butadiene/Schiff Base

Ligand-Assisted Catalysis: New Active and Selective Nickel Modified Homogeneous Catalysts for Linear Dimerization of Butadiene

Denis, Philippe,Mortreux, Andre,Petit, Francis,Buono, Gerard,Peiffer, Gilbert

, p. 5274 - 5276 (2007/10/02)

New aminophosphinite-modified Ni(0) catalysts have been found to be the most active ever described for linear dimerization of butadiene, affording almost exclusively 1,3,6- and 2,4,6-octatrienes, according to the reaction conditions.

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