nona-3,4-diene-1,5-diyldibenzene

Base Information

Chemical Name:nona-3,4-diene-1,5-diyldibenzene
CAS No.:1354723-35-5
Molecular Formula:C₂₁H₂₄
Molecular Weight:276.422
Hs Code.:

Synonyms:nona-3,4-diene-1,5-diyldibenzene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of nona-3,4-diene-1,5-diyldibenzene

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Technology Process of nona-3,4-diene-1,5-diyldibenzene

There total 7 articles about nona-3,4-diene-1,5-diyldibenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 1354723-14-0
diphenyl 1-phenyl-4-nonynyl phosphate

: 5123-13-7
5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane

: 1354723-35-5
nona-3,4-diene-1,5-diyldibenzene

Guidance literature:: With potassium tert-butylate; water; copper(l) chloride; In acetonitrile; at 60 ℃; for 4h; stereospecific reaction; Inert atmosphere;
DOI:10.1021/ol2033465

Reference yield: 68.0%

: 591-50-4
iodobenzene

: 1082069-11-1
methyl 1-phenyl-4-nonyn-3-yl carbonate

: 1354723-35-5
nona-3,4-diene-1,5-diyldibenzene

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; tetrahydroxydiboron; sodium carbonate; copper(l) chloride; In methanol; toluene; at 20 ℃; for 16h; Reagent/catalyst; Solvent; Inert atmosphere; Glovebox; Sealed tube;
DOI:10.1021/acs.joc.5b01842

Reference yield: 60.0%

: 1831-57-8
2-phenyl-4,4,5,5-tetramethyl-1,3-dioxolane

: 1354723-14-0
diphenyl 1-phenyl-4-nonynyl phosphate

: 1354723-35-5
nona-3,4-diene-1,5-diyldibenzene

Guidance literature:: With potassium tert-butylate; water; copper(l) chloride; In acetonitrile; at 60 ℃; for 4h; stereospecific reaction; Inert atmosphere;
DOI:10.1021/ol2033465