[(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane

Base Information

Chemical Name:[(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane
CAS No.:87997-17-9
Molecular Formula:C₂₂H₁₇N₂O₃P
Molecular Weight:388.362
Hs Code.:
DSSTox Substance ID:DTXSID00518493
Wikidata:Q82381198

Synonyms:87997-17-9;DTXSID00518493;[(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane

Suppliers and Price of [(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of [(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane

Chemical Property:

XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:388.09767941
Heavy Atom Count:28
Complexity:521

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)P(=NC2=CC=C(O2)[N+](=O)[O-])(C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of [(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane

There total 2 articles about [(5-Nitrofuran-2-yl)imino](triphenyl)-lambda~5~-phosphane 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%

: 87997-15-7
5-nitro-2-furyl azide

: 603-35-0
triphenylphosphine

: 87997-17-9
2-(N-iminotriphenylphosphorano)-5-nitrofuran

Guidance literature:: In diethyl ether;

Reference yield:

: 87997-10-2
5-nitro-2-furyltrimethylammonium bromide

: 87997-17-9
2-(N-iminotriphenylphosphorano)-5-nitrofuran

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / NaN₃ / diethyl ether; H₂O

2: 98 percent / diethyl ether

With sodium azide; In diethyl ether; water;