Acridophosphine,10-phenyl-

Base Information

Chemical Name:Acridophosphine,10-phenyl-
CAS No.:20995-81-7
Molecular Formula:C₁₉H₁₃P
Molecular Weight:272.286
Hs Code.:2902909090
DSSTox Substance ID:DTXSID40175206
Nikkaji Number:J83.050J
Wikidata:Q83045480
Mol file:20995-81-7.mol

Synonyms:Acridophosphine,10-phenyl-;20995-81-7;10-phenylacridophosphine;DTXSID40175206

Suppliers and Price of Acridophosphine,10-phenyl-

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 3 raw suppliers

Chemical Property of Acridophosphine,10-phenyl-

Chemical Property:

PSA：34.14000
LogP:3.76990
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:272.075487412
Heavy Atom Count:20
Complexity:298

Purity/Quality:: 99% ^*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=C3C=CC=CC3=PC4=CC=CC=C42

Technology Process of Acridophosphine,10-phenyl-

There total 8 articles about Acridophosphine,10-phenyl- 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:

: 20995-83-9
5-chloro-10-phenyl-5,10-dihydro-acridophosphine

: 20995-81-7
10-phenyl-acridophosphine

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide;

Reference yield:

: 20995-82-8
(2-benzhydryl-phenyl)-phosphonous acid dichloride

: 20995-81-7
10-phenyl-acridophosphine

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃ / CS₂ / Heating

2: DBU / dimethylformamide

With aluminium trichloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In carbon disulfide; N,N-dimethyl-formamide;