1-(9h-Fluoren-2-yl)ethanol

Base Information

Chemical Name:1-(9h-Fluoren-2-yl)ethanol
CAS No.:20371-86-2
Molecular Formula:C15H14 O
Molecular Weight:210.276
Hs Code.:
NSC Number:102367
Nikkaji Number:J2.195.177C

Synonyms:20371-86-2;1-(9h-fluoren-2-yl)ethanol;1-(9H-FLUOREN-2-YL)ETHAN-1-OL;2-(1-hydroxyethyl)-9H-fluorene;NSC102367;2-(1-hydroxyethyl)fluorene;NCIOpen2_007034;SCHEMBL7642376;SDSFBEANHZINLH-UHFFFAOYSA-N;AKOS000125208;NSC-102367;CS-0352313;FT-0716537;Z228586194

Suppliers and Price of 1-(9h-Fluoren-2-yl)ethanol

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 4 raw suppliers

Chemical Property of 1-(9h-Fluoren-2-yl)ethanol

Chemical Property:

Vapor Pressure:2.52E-06mmHg at 25°C
Boiling Point:376.1°C at 760 mmHg
Flash Point:167.7°C
Density:1.172g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:210.104465066
Heavy Atom Count:16
Complexity:250

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC2=C(C=C1)C3=CC=CC=C3C2)O

Technology Process of 1-(9h-Fluoren-2-yl)ethanol

There total 4 articles about 1-(9h-Fluoren-2-yl)ethanol 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: 82.0%

: 781-73-7
1-(9H-fluoren-2-yl)ethanone

: 20371-86-2
1-(9H-fluoren-2-yl)ethan-1-ol

Guidance literature:: With sodium hypophosphite monohydrate; 5%-palladium/activated carbon; tetrabutyl-ammonium chloride; In 2-methyltetrahydrofuran; water; at 60 ℃; for 7h; Schlenk technique;
DOI:10.1016/j.tet.2014.02.014

Reference yield: 20.0%

: 75-69-4
trichlorofluoromethane

: 2-(1,1-Dimethoxy-ethyl)-9H-fluorene

: 36950-96-6
2-(2fluorenyl)propionic acid

: 20371-86-2
1-(9H-fluoren-2-yl)ethan-1-ol

: C₃₀H₂₄

Guidance literature:: With lithium aluminium tetrahydride; titanium(IV) iodide; In tetrahydrofuran; at -5 ℃; for 0.5h;

Reference yield:

: 86-73-7
9H-fluorene

: 20371-86-2
1-(9H-fluoren-2-yl)ethan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃; carbon disulfide

2: copper oxide-chromium oxide; ethanol / 130 °C / 55163.1 - 95616 Torr / Hydrogenation

With carbon disulfide; aluminium trichloride; ethanol; copper oxide-chromium oxide;