5-(4-fluorophenyl)-1H-indole

Base Information

Chemical Name:5-(4-fluorophenyl)-1H-indole
CAS No.:144104-44-9
Molecular Formula:C14H10 F N
Molecular Weight:211.239
Hs Code.:
DSSTox Substance ID:DTXSID70457603
Nikkaji Number:J2.191.804K
Mol file:144104-44-9.mol

Synonyms:5-(4-fluorophenyl)-1H-indole;144104-44-9;5-(4-Fluoro-phenyl)-1H-indole;1H-Indole, 5-(4-fluorophenyl)-;SCHEMBL856313;DTXSID70457603;FZEPXXHITBIOIY-UHFFFAOYSA-N;AKOS004118861;AC-18716;BB 0223583;4-chloro-2-(4-tolylsulphonyl)anthranilicacid;A1-02468

Suppliers and Price of 5-(4-fluorophenyl)-1H-indole

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

American Custom Chemicals Corporation
5-(4-FLUORO-PHENYL)-1H-INDOLE 95.00%
5MG
$ 497.74

Alichem
5-(4-Fluorophenyl)-1H-indole
5g
$ 1076.67

Alichem
5-(4-Fluorophenyl)-1H-indole
1g
$ 510.00

A1 Biochem Labs
5-(4-Fluoro-phenyl)-1H-indole 95%
1 g
$ 450.00

Total 16 raw suppliers

Chemical Property of 5-(4-fluorophenyl)-1H-indole

Chemical Property:

Vapor Pressure:6.55E-06mmHg at 25°C
Refractive Index:1.658
Boiling Point:389.1°C at 760 mmHg
Flash Point:189.1°C
PSA：15.79000
Density:1.232g/cm³
LogP:3.97400
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:211.079727485
Heavy Atom Count:16
Complexity:235

Purity/Quality:

99% ^*data from raw suppliers

5-(4-FLUORO-PHENYL)-1H-INDOLE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=CC3=C(C=C2)NC=C3)F

Technology Process of 5-(4-fluorophenyl)-1H-indole

There total 6 articles about 5-(4-fluorophenyl)-1H-indole 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: 98.0%

: 10075-50-0
5-bromo-1H-indole

: 1765-93-1
4-fluoroboronic acid

: 144104-44-9
5-(4-fluoro-phenyl)-1H-indole

Guidance literature:: With dihydrogen dichloro-bis(di-tert-butylphosphinito-κP)palladium(2-); tetrabutylammomium bromide; potassium hydroxide; In water; for 8h; Inert atmosphere; Schlenk technique;
DOI:10.1007/s13738-015-0775-9

Reference yield: 77.0%

: 160874-85-1
2-(4-fluorophenyl)-[1,3,2]-dioxaborolane

: 10075-50-0
5-bromo-1H-indole

: 144104-44-9
5-(4-fluoro-phenyl)-1H-indole

Guidance literature:: With tris [tris(3,5-bis(trifluoromethyl)phenyl)phosphine]palladium⁽⁰⁾; potassium carbonate; In methanol; water; at 110 ℃; for 1h;
DOI:10.1002/ejoc.201403214