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PF-03715455

Base Information
  • Chemical Name:PF-03715455
  • CAS No.:1056164-52-3
  • Molecular Formula:C35H34ClN7O3S2
  • Molecular Weight:700.285
  • Hs Code.:
  • UNII:0TJ631J0KP
  • ChEMBL ID:CHEMBL1938400
  • DSSTox Substance ID:DTXSID70147214
  • Metabolomics Workbench ID:153182
  • Pharos Ligand ID:NRPY9K4LX7NJ
  • Wikidata:Q27088311
PF-03715455

Synonyms:N-(1-(3-chloro-4-hydroxyphenyl)-3-(1,1-dimethylethyl)-1H-pyrazol-5-yl)-N'-((2-((3-(2-((2-hydroxyethyl)thio)phenyl)-1,2,4-triazolo(4,3-a)pyridin-6-yl)thio)phenyl)methyl)-urea;PF 03715455;PF-03715455;PF-3715455;PF03715455

Suppliers and Price of PF-03715455
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
  • DC Chemicals
  • PF03715455 >98%
  • 5mg
  • $ 850.00
Total 2 raw suppliers
Chemical Property of PF-03715455
Chemical Property:
  • Melting Point:220 °C 
  • Density:1.39±0.1 g/cm3(Predicted) 
  • XLogP3:7.5
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:11
  • Exact Mass:699.1853080
  • Heavy Atom Count:48
  • Complexity:1040
Purity/Quality:

95% *data from raw suppliers

PF03715455 >98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)(C)C1=NN(C(=C1)NC(=O)NCC2=CC=CC=C2SC3=CN4C(=NN=C4C5=CC=CC=C5SCCO)C=C3)C6=CC(=C(C=C6)O)Cl
  • Recent ClinicalTrials:An Evaluation Of PF-03715455 In Moderate To Severe Uncontrolled Asthma
  • Recent EU Clinical Trials:A Randomized, Double-Blind, Placebo-Controlled 2-Way Crossover Study to Evaluate the Efficacy, Safety and Tolerability of PF-03715455 Administered Twice Daily By Inhalation for 4 Weeks in Subjects with Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)
Technology Process of PF-03715455

There total 10 articles about PF-03715455 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:
Guidance literature:
Multi-step reaction with 2 steps
1: dimethyl sulfoxide / 20 °C / Inert atmosphere
2: triethylamine tris(hydrogen fluoride) / methanol / 20 °C / Inert atmosphere
With triethylamine tris(hydrogen fluoride); In methanol; dimethyl sulfoxide;
DOI:10.1021/jm200677b
Guidance literature:
Multi-step reaction with 2 steps
1: dimethyl sulfoxide / 20 °C / Inert atmosphere
2: triethylamine tris(hydrogen fluoride) / methanol / 20 °C / Inert atmosphere
With triethylamine tris(hydrogen fluoride); In methanol; dimethyl sulfoxide;
DOI:10.1021/jm200677b
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