2-Phenylfuro[2,3-b]quinoxaline

Base Information

Chemical Name:2-Phenylfuro[2,3-b]quinoxaline
CAS No.:37052-98-5
Molecular Formula:C16H10N2O
Molecular Weight:246.268
Hs Code.:
NSC Number:99094
DSSTox Substance ID:DTXSID00294982
Nikkaji Number:J3.200.337K
Wikidata:Q82034630

Synonyms:2-phenylfuro[2,3-b]quinoxaline;37052-98-5;NSC99094;DTXSID00294982;NSC-99094;AKOS024360303

Suppliers and Price of 2-Phenylfuro[2,3-b]quinoxaline

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 2-Phenylfuro[2,3-b]quinoxaline

Chemical Property:

Vapor Pressure:1.23E-07mmHg at 25°C
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:246.079312947
Heavy Atom Count:19
Complexity:316

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC3=NC4=CC=CC=C4N=C3O2

Technology Process of 2-Phenylfuro[2,3-b]quinoxaline

There total 19 articles about 2-Phenylfuro[2,3-b]quinoxaline 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: 93.0%

: 924-44-7
glyoxylic acid ethyl ester

: 536-74-3
phenylacetylene

: 95-54-5
1,2-diamino-benzene

: 37052-98-5
2-phenylfuro<2,3-b>quinoxaline

Guidance literature:: With Cu(OTf)₂ loaded protonated trititanate nanotubes; In toluene; at 100 ℃; for 0.333333h; Solvent; Reagent/catalyst; Temperature; Catalytic behavior;
DOI:10.1039/c8nj00287h