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Ulipristal

Base Information Edit
  • Chemical Name:Ulipristal
  • CAS No.:159811-51-5
  • Molecular Formula:C28H35 N O3
  • Molecular Weight:433.591
  • Hs Code.:
  • European Community (EC) Number:815-032-8
  • UNII:6J5J15Q2X8
  • ChEMBL ID:CHEMBL2103846
  • DSSTox Substance ID:DTXSID501025842
  • Metabolomics Workbench ID:151964
  • NCI Thesaurus Code:C91056
  • Pharos Ligand ID:SQMHQGH31URQ
  • RXCUI:1005921
  • Wikidata:Q27264992
  • Mol file:159811-51-5.mol
Ulipristal

Synonyms:CDB3236; Deacetyl CDB 2914; Ulipristal

Suppliers and Price of Ulipristal
Supply Marketing:Edit
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
  • TRC
  • Ulipristal
  • 100mg
  • $ 1455.00
  • TRC
  • Ulipristal
  • 10mg
  • $ 185.00
  • Crysdot
  • Ulipristal 97%
  • 50mg
  • $ 585.00
  • Crysdot
  • Ulipristal 97%
  • 25mg
  • $ 315.00
  • American Custom Chemicals Corporation
  • CDB-3236 95.00%
  • 5G
  • $ 1005.43
  • American Custom Chemicals Corporation
  • CDB-3236 95.00%
  • 2.5G
  • $ 852.21
  • American Custom Chemicals Corporation
  • CDB-3236 95.00%
  • 1G
  • $ 648.81
Total 113 raw suppliers
Chemical Property of Ulipristal Edit
Chemical Property:
  • Melting Point:183.5-184.5oC /Losartan/ 
  • Boiling Point:638.5±55.0 °C(Predicted) 
  • PKA:12.94±0.60(Predicted) 
  • PSA:57.61000 
  • Density:1.20 
  • LogP:4.97220 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:433.26169398
  • Heavy Atom Count:32
  • Complexity:877
Purity/Quality:

99% *data from raw suppliers

Ulipristal *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)C1(CCC2C1(CC(C3=C4CCC(=O)C=C4CCC23)C5=CC=C(C=C5)N(C)C)C)O
  • Isomeric SMILES:CC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H](C3=C4CCC(=O)C=C4CC[C@@H]23)C5=CC=C(C=C5)N(C)C)C)O
  • Recent ClinicalTrials:UA Versus UAE in Treatment of Fibroids
  • Recent EU Clinical Trials:A Phase III, multicentre, clinical study investigating the efficacy and safety of three successive periods of 3-month open-label PGL4001 treatment, each followed by ten days of double-blind treatment with progestin or placebo and a drug-free period until return of menses, in subjects with myomas and heavy uterine bleeding.
  • Recent NIPH Clinical Trials:Phase III Clinical Study to Evaluate Efficacy and Safety of CDB-2914 Compared with Leuprorelin Acetate in Patients with Uterine Myoma
  • Uses Labelled Ulipristal. Ulipristal is a selective progesterone receptor modulator. Ulipristal is used during pregnancy. Labelled Ulipristal (U700800). Ulipristal is a selective progesterone receptor modulator. Ulipristal is used during pregnancy. Α selective progesterone receptor modulator
Technology Process of Ulipristal

There total 33 articles about Ulipristal 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: 98.2%

Guidance literature:
With hydrogenchloride; In methanol; water; at 20 ℃; for 1h; Industrial scale;
Guidance literature:
With acetic acid; In water; at 25 ℃; for 1h;
Refernces Edit
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