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Parahydroxyatorvastatin

Base Information Edit
  • Chemical Name:Parahydroxyatorvastatin
  • CAS No.:214217-88-6
  • Molecular Formula:C33H35 F N2 O6
  • Molecular Weight:574.649
  • Hs Code.:
  • UNII:9Q2QX99L5W
  • Nikkaji Number:J996.541F
  • Wikidata:Q27088372
  • Mol file:214217-88-6.mol
Parahydroxyatorvastatin

Synonyms:4-hydroxy-atorvastatin;4-hydroxyatorvastatin

Suppliers and Price of Parahydroxyatorvastatin
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
  • Usbiological
  • 4-Hydroxy atorvastatin disodium salt
  • 1mg
  • $ 531.00
  • Medical Isotopes, Inc.
  • p-HydroxyAtorvastatin-d5
  • 1 mg
  • $ 1400.00
  • Medical Isotopes, Inc.
  • 4-Hydroxyatorvastatincalcium-d5
  • 1 mg
  • $ 720.00
  • Biosynth Carbosynth
  • Disodium (3R,5R)-7-{2-(4-Fluorophenyl)-5-Isopropyl-4-[(4-Oxidophenyl)Carbamoyl]-3-Phenyl-1H-Pyrrol-1-Yl}-3,5-Dihydroxyheptanoate
  • 2 mg
  • $ 375.00
  • Biosynth Carbosynth
  • Disodium (3R,5R)-7-{2-(4-Fluorophenyl)-5-Isopropyl-4-[(4-Oxidophenyl)Carbamoyl]-3-Phenyl-1H-Pyrrol-1-Yl}-3,5-Dihydroxyheptanoate
  • 1 mg
  • $ 220.00
  • Biosynth Carbosynth
  • Disodium (3R,5R)-7-{2-(4-Fluorophenyl)-5-Isopropyl-4-[(4-Oxidophenyl)Carbamoyl]-3-Phenyl-1H-Pyrrol-1-Yl}-3,5-Dihydroxyheptanoate
  • 10 mg
  • $ 1300.00
  • Biosynth Carbosynth
  • Disodium (3R,5R)-7-{2-(4-Fluorophenyl)-5-Isopropyl-4-[(4-Oxidophenyl)Carbamoyl]-3-Phenyl-1H-Pyrrol-1-Yl}-3,5-Dihydroxyheptanoate
  • 5 mg
  • $ 750.00
  • Biosynth Carbosynth
  • Disodium (3R,5R)-7-{2-(4-Fluorophenyl)-5-Isopropyl-4-[(4-Oxidophenyl)Carbamoyl]-3-Phenyl-1H-Pyrrol-1-Yl}-3,5-Dihydroxyheptanoate
  • 25 mg
  • $ 2950.00
  • American Custom Chemicals Corporation
  • PARA-HYDROXY ATORVASTATIN CALCIUM SALT 95.00%
  • 10MG
  • $ 1612.96
  • American Custom Chemicals Corporation
  • PARA-HYDROXY ATORVASTATIN CALCIUM SALT 95.00%
  • 1MG
  • $ 679.14
Total 6 raw suppliers
Chemical Property of Parahydroxyatorvastatin Edit
Chemical Property:
  • Melting Point:183-185°C 
  • Boiling Point:759.0±60.0 °C(Predicted) 
  • PKA:4.29±0.10(Predicted) 
  • PSA:242.04000 
  • Density:1.27±0.1 g/cm3(Predicted) 
  • LogP:12.03020 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:Methanol (Slightly) 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:12
  • Exact Mass:574.24791500
  • Heavy Atom Count:42
  • Complexity:854
Purity/Quality:

98%Min *data from raw suppliers

4-Hydroxy atorvastatin disodium salt *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=C(C=C4)O
  • Isomeric SMILES:CC(C)C1=C(C(=C(N1CC[C@H](C[C@H](CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=C(C=C4)O
  • Uses Atorvastatin metabolite
Technology Process of Parahydroxyatorvastatin

There total 10 articles about Parahydroxyatorvastatin 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:
With chimera No.17A1V2 derived from CYP102A1 mutant; In aq. phosphate buffer; dimethyl sulfoxide; Reagent/catalyst; Catalytic behavior; Enzymatic reaction;
Guidance literature:
Multi-step reaction with 7 steps
1: 82 percent / toluene / Heating
2: β-alanine; glacial acetic acid / hexane / Heating
3: 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide; triethylamine / ethanol / Heating
4: pivalic acid / tetrahydrofuran; toluene; heptane / Heating
5: 85 percent / hydrogen; acetic acid / palladium on carbon / ethyl acetate / 34 h / 2585.74 Torr
6: HCl / tetrahydrofuran; H2O / 20 °C
7: sodium hydroxide / H2O; tetrahydrofuran / 20 °C
With hydrogenchloride; sodium hydroxide; hydrogen; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; acetic acid; triethylamine; 3-amino propanoic acid; Trimethylacetic acid; palladium on activated charcoal; In tetrahydrofuran; ethanol; hexane; n-heptane; water; ethyl acetate; toluene; 1: Acylation / 2: Condensation / 3: Addition / 4: Cycloaddition / 5: Hydrogenolysis / 6: Hydrolysis / 7: Hydrolysis;
DOI:10.1002/(SICI)1099-1344(20000315)43:3<261::AID-JLCR312>3.0.CO;2-T
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