Hexahelicene

Base Information

Chemical Name:Hexahelicene
CAS No.:187-83-7
Molecular Formula:C₂₆H₁₆
Molecular Weight:328.413
Hs Code.:
NSC Number:171474
UNII:G5UR49H4NR
DSSTox Substance ID:DTXSID80171964
Nikkaji Number:J5.874B
Wikidata:Q3135032
Metabolomics Workbench ID:54835
Mol file:187-83-7.mol

Synonyms:helicenes;hexahelicene

Suppliers and Price of Hexahelicene

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

TRC
Hexahelicene
5mg
$ 1320.00

American Custom Chemicals Corporation
(6)-HELICENE 98.00%
100MG
$ 2625.00

American Custom Chemicals Corporation
(6)-HELICENE 98.00%
10MG
$ 1007.25

Total 20 raw suppliers

Chemical Property of Hexahelicene

Chemical Property:

Vapor Pressure:6.64E-14mmHg at 25°C
Melting Point:263-267 °C
Boiling Point:604.1°Cat760mmHg
Flash Point:314.6°C
PSA：0.00000
Density:1.263g/cm³
LogP:7.45260
Storage Temp.:-20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly, Sonicated)
XLogP3:7.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:328.125200510
Heavy Atom Count:26
Complexity:464

Purity/Quality:

97% ^*data from raw suppliers

Hexahelicene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC3=C2C4=C(C=C3)C=CC5=C4C6=CC=CC=C6C=C5
Uses Hexahelicene, can be used in asymmetric polymerization of triphenylmethyl methacrylate by C2-chiral catalysts.

Technology Process of Hexahelicene

There total 38 articles about Hexahelicene 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: 92.0%

: 1,8-bis{2-[(1,3-dioxolan-2- yl)methyl]phenyl}naphthalene

: 187-83-7,17486-32-7,19253-33-9
[6]helicene

Guidance literature:: With trifluorormethanesulfonic acid; at 0 - 20 ℃; for 0.666667h;
DOI:10.3762/BJOC.17.35

Reference yield: 86.0%

: 457885-37-9
2-[(1Z)-1-buten-3-ynyl]-1-({2-[(1Z)-1-buten-3-ynyl]phenyl}ethynyl)naphthalene

: 187-83-7,17486-32-7,19253-33-9
[6]helicene

Guidance literature:: bis(1,5-cyclooctadiene)nickel ⁽⁰⁾; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/ja0259584

Reference yield: 85.0%

: 20508-11-6
(Z)-1-Phenyl-2-(2-benzophenanthrenyl)ethylene

: 20508-12-7
(E)-1-Phenyl-2-(2-benzophenanthrenyl)ethylene

: 187-83-7,17486-32-7,19253-33-9
[6]helicene

Guidance literature:: With cholesteryl tetradecanoate; iodine; cholesteryl chloride; In neat (no solvent); at 80 ℃; for 2h; Irradiation;
DOI:10.1021/jo01314a044