Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)-

Base Information

Chemical Name:Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)-
CAS No.:52333-94-5
Molecular Formula:C12H7FN2O
Molecular Weight:214.2
Hs Code.:2934999090
DSSTox Substance ID:DTXSID30200359
Nikkaji Number:J78.701I
Wikidata:Q83073452
ChEMBL ID:CHEMBL3244996
Mol file:52333-94-5.mol

Synonyms:52333-94-5;II-13;Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)-;BRN 0523683;2-(2-Fluorophenyl)oxazolo(5,4-b)pyridine;Oxazolo[5,4-b]pyridine, 2-(2-fluorophenyl)-;2-(2-fluorophenyl)oxazolo[5,4-b]pyridine;SCHEMBL9867369;CHEMBL3244996;DTXSID30200359;BYWCPISMBVLTKQ-UHFFFAOYSA-N;LS-100851

Suppliers and Price of Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)-

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

Usbiological
H13
100ul
$ 499.00

American Custom Chemicals Corporation
2-(2-FLUOROPHENYL)OXAZOLO[5,4-B]PYRIDINE 95.00%
5MG
$ 501.26

Total 4 raw suppliers

Chemical Property of Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)-

Chemical Property:

Vapor Pressure:0.00129mmHg at 25°C
Boiling Point:307.8°C at 760 mmHg
Flash Point:139.9°C
PSA：38.92000
Density:1.319g/cm³
LogP:3.02890
Storage Temp.:-20°C
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:214.05424101
Heavy Atom Count:16
Complexity:251

Purity/Quality:

99% ^*data from raw suppliers

H13 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C2=NC3=C(O2)N=CC=C3)F

Technology Process of Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)-

There total 6 articles about Oxazolo(5,4-b)pyridine, 2-(2-fluorophenyl)- 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%

: 126921-76-4
3-(2-fluorobenzoylamino)-2-chloropyridine

: 52333-94-5
2-(2-fluoro-phenyl)oxazolo<5,4-b>pyridine

Guidance literature:: With trimethylsilylpolyphosphate ester; In various solvent(s); for 15h; Heating;

Reference yield:

: 52334-52-8
3-(2-fluoro-benzoylamino)-1H-pyridin-2-one

: 52333-94-5
2-(2-fluoro-phenyl)oxazolo<5,4-b>pyridine

Guidance literature:: With trichlorophosphate;
DOI:10.1021/jm00209a014

Reference yield:

: 393-52-2
2-Fluorobenzoyl chloride

: 52333-94-5
2-(2-fluoro-phenyl)oxazolo<5,4-b>pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / pyridine / 1. -10 deg C 2. 15 h r. t.

2: 98 percent / trimethylsilylpolyphosphate ester (PPSE) / various solvent(s) / 15 h / Heating

With trimethylsilylpolyphosphate ester; In pyridine;