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1,6-bis(phenyl)-3,4-bis(phenylethynyl)hex-3-ene-1,5-diyne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17531-26-9

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17531-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17531-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,3 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17531-26:
(7*1)+(6*7)+(5*5)+(4*3)+(3*1)+(2*2)+(1*6)=99
99 % 10 = 9
So 17531-26-9 is a valid CAS Registry Number.

17531-26-9Relevant academic research and scientific papers

Substituted Tetraethynylethylene–Tetravinylethylene Hybrids

Connor, Kieran P. E.,Horvath, Kelsey L.,Magann, Nicholas L.,Sherburn, Michael S.,Sowden, Madison J.,Westley, Erin

supporting information, p. 977 - 986 (2022/02/03)

A general synthetic approach to molecular structures that are hybrids of tetraethynylethylene (TEE) and tetravinylethylene (TVE) is reported. The synthesis permits the controlled preparation of many previously inaccessible structures, including examples w

Radical Reactions of 1,4-Alkadiynes: Metal Coordination as an Effective Tool for Controlling the Regio- and Stereoselectivity of the C-C Bond Formation

Melikyan, Gagik G.,Anker, Bryan

supporting information, p. 4194 - 4197 (2015/09/22)

A novel method for selective generation of radicals in 1,4-alkadiynes is developed by employing a π-bonded Co2(CO)6 core as a triple-bond immobilizing, cation-stabilizing, and radical-guiding auxiliary group. The isolation of α-alkyn

A simple synthesis of tetraethynylethenes and representative molecular structures of some dicobalt derivatives

Koentjoro, Olivia F.,Zuber, Philipp,Puschmann, Horst,Goeta, Andres E.,Howard, Judith A.K.,Low, Paul J.

, p. 178 - 187 (2007/10/03)

Palladium-copper catalysed cross-coupling reactions of tetracholoroethene with terminal acetylenes RC≡CH (R = SiMe3, C6H5, C6H4CN-4) in refluxing triethylamine afford the corresponding tetraethynylethenes in 30-60% isolated yields. The reaction of 1,6- bis(trimethylsilyl)-3,4-bis (trimethylsilylethynyl)-hex-3-ene-1,5-diyne with [Co2(CO)6(L2)] [L2 = (CO)2 or μ-dppm] affords complexes in which one or two (trans) acetylene moieties are coordinated by a dicobalt fragment.

?-Complexes incorporating tetrakis(phenylethynyl)ethene

Philp, Douglas,Gramlich, Volker,Seiler, Paul,Diederich, Francois

, p. 875 - 886 (2007/10/02)

Tetrakis(phenylethynyl)ethene and the ?-acceptors 2,4,7-trinitrofluoren-9-one and (2,4,7-trinitrofluoren-9-ylidene)malononitrile form highly ordered donor-acceptor ?-complexes having 1:2 stoichiometry in the solid state.In solution, relatively weak 1:1 co

?-Complexes incorporating Tetraphenyltetraethynylethene

Diederich, Francois,Philp, Douglas,Seiler, Paul

, p. 205 - 208 (2007/10/02)

Tetraphenyltetraethynylethene and the ?-acceptors 2,4,7-trinitrofluoren-9-one and (2,4,7-trinitro-9-fluorenylidene)malononitrile form highly ordered donor-acceptor ?-complexes having 1:2 stoichiometry in the solid state; in solution, relatively weak 1:1 c

New Planar ?-Systems, II. - On the Preparation and Structure of Tetrakis(phenylethynyl)ethene

Hopf, Henning,Kreutzer, Martin,Jones, Peter G.

, p. 1471 - 1475 (2007/10/02)

The preparation of tetrakis(phenylethynyl)ethene (1b) has been repeated.Among various routes to this highly unsaturated cross-conjugated ?-system, the dimerization of bromide 2 via the carbene 3 is the most simple one.Full spectroscopic data for 1b are re

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