8-Triphenylmethoxy-1-octyne

Base Information

Chemical Name:8-Triphenylmethoxy-1-octyne
CAS No.:52517-97-2
Molecular Formula:C27H28O
Molecular Weight:368.519
Hs Code.:
DSSTox Substance ID:DTXSID10606476
Wikidata:Q82505252
Mol file:52517-97-2.mol

Synonyms:8-triphenylmethoxy-1-octyne;52517-97-2;8-triphenylmethoxy-1octyne;SCHEMBL5326522;DTXSID10606476;ZPLVYMJBYVKANF-UHFFFAOYSA-N;1,1',1''-{[(Oct-7-yn-1-yl)oxy]methanetriyl}tribenzene

Suppliers and Price of 8-Triphenylmethoxy-1-octyne

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 8-Triphenylmethoxy-1-octyne

Chemical Property:

XLogP3:7.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:10
Exact Mass:368.214015512
Heavy Atom Count:28
Complexity:408

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C#CCCCCCCOC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 8-Triphenylmethoxy-1-octyne

There total 6 articles about 8-Triphenylmethoxy-1-octyne 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:

: ((6-chlorohexyloxy)methanetriyl)tribenzene

ether-pet ether: ether-pet ether

: 2009-83-8
6-chloro-1-hexanol

: 76-83-5
trityl chloride

: 52517-97-2
1-triphenylmethyloxyoct-7-yne

Guidance literature:: With hydrogenchloride; In water; dimethyl sulfoxide;

Reference yield:

: 629-11-8
1,6-hexanediol

: 52517-97-2
1-triphenylmethyloxyoct-7-yne

Guidance literature:: Multi-step reaction with 4 steps

1: 48 percent / iron (III) sulphate on silica gel / hexane / 1.42 h / 45 °C

2: 84 percent / pyridine / CH₂Cl₂ / 16 h / Ambient temperature

3: 46 percent / I₂, 1,2-bis(diphenylphosphino)ethane / CH₂Cl₂ / 4 h / Ambient temperature

4: 34 percent / dimethylsulfoxide / 2 h / Ambient temperature

With pyridine; iodine; 1,2-bis-(diphenylphosphino)ethane; iron(III) sulfate; In hexane; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/0009-3084(94)90067-1

Reference yield:

: 28659-22-5
6-(tetrahydro-2H-pyranyloxy)hexan-1-ol

: 52517-97-2
1-triphenylmethyloxyoct-7-yne

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / pyridine / CH₂Cl₂ / 16 h / Ambient temperature

2: 46 percent / I₂, 1,2-bis(diphenylphosphino)ethane / CH₂Cl₂ / 4 h / Ambient temperature

3: 34 percent / dimethylsulfoxide / 2 h / Ambient temperature

With pyridine; iodine; 1,2-bis-(diphenylphosphino)ethane; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/0009-3084(94)90067-1