Pyriprole

Base Information

Chemical Name:Pyriprole
CAS No.:394730-71-3
Molecular Formula:C18H10Cl2F5N5S
Molecular Weight:494.275
Hs Code.:
European Community (EC) Number:881-741-4
UNII:69OX73ZVJN
DSSTox Substance ID:DTXSID20192613
Nikkaji Number:J2.466.569K
Wikidata:Q3905626
Wikipedia:Pyriprole

Synonyms:pyriprole

Suppliers and Price of Pyriprole

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 18 raw suppliers

Chemical Property of Pyriprole

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:517.748°C at 760 mmHg
Flash Point:266.925°C
Density:1.588g/cm³
XLogP3:6.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:6
Exact Mass:492.9954127
Heavy Atom Count:31
Complexity:639

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=NC(=C1)CNC2=C(C(=NN2C3=C(C=C(C=C3Cl)C(F)(F)F)Cl)C#N)SC(F)F

Technology Process of Pyriprole

There total 2 articles about Pyriprole 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: 94.0%

: C₁₇H₁₀Cl₂F₃N₅

: 2-((difluoromethyl)thio)isoindoline-1,3-dione

: 394730-71-3
1-(2,6-dichloro-alpha,alpha,alpha-trifluoro-p-tolyl)-4-(difluoromethylthio)-5-[(2-pyridylmethyl)amino]pyrazole-3-carbonitrile

Guidance literature:: With sodium chloride; In N,N-dimethyl-formamide; at 80 ℃; for 16h; Reagent/catalyst; Solvent; Schlenk technique; Inert atmosphere;
DOI:10.1021/jacs.5b03170