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Pfhmv-D3

Base Information
  • Chemical Name:Pfhmv-D3
  • CAS No.:119839-97-3
  • Molecular Formula:C28H41F5O3
  • Molecular Weight:520.624
  • Hs Code.:
  • Mol file:119839-97-3.mol
Pfhmv-D3

Synonyms:26,26,26,27,27-pentafluoro-1-hydroxy-27-methoxyvitamin D3;PFHMV-D3

Suppliers and Price of Pfhmv-D3
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
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Total 1 raw suppliers
Chemical Property of Pfhmv-D3
Chemical Property:
  • Vapor Pressure:7.11E-14mmHg at 25°C 
  • Boiling Point:539.2°Cat760mmHg 
  • Flash Point:230.5°C 
  • PSA:49.69000 
  • Density:1.17g/cm3 
  • LogP:7.35150 
  • XLogP3:7.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:8
  • Exact Mass:520.29758598
  • Heavy Atom Count:36
  • Complexity:849
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CCCC(C(OC)(F)F)C(F)(F)F)C1CCC2C1(CCCC2=CC=C3CC(CC(C3=C)O)O)C
  • Isomeric SMILES:C[C@H](CCCC(C(OC)(F)F)C(F)(F)F)C1CCC\2[C@@]1(CCC/C2=C\C=C/3\C[C@H](CC(C3=C)O)O)C
Technology Process of Pfhmv-D3

There total 5 articles about Pfhmv-D3 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 5 steps
1: triphenylphosphine / diethyl ether / 16 h / -78 °C
2: 51 percent / sodium borohydride / tetrahydrofuran; 2-methyl-propan-2-ol / 22 h / Ambient temperature
3: 1.) N-bromosuccinimide; 2.) collidine/xylene / CCl4 / 1.) reflux, 25 min; 2.) reflux, 20 min
4: 20 percent / 5percent potassium hydroxyde / tetrahydrofuran / 1 h / Ambient temperature
5: 15 percent / benzene; ethanol / 1.) irrad., 5 min; 2.) reflux, 1 h
With 2,3,5-trimethyl-pyridine; potassium hydroxide; sodium tetrahydroborate; N-Bromosuccinimide; triphenylphosphine; xylene; In tetrahydrofuran; tetrachloromethane; diethyl ether; ethanol; tert-butyl alcohol; benzene;
DOI:10.1248/cpb.36.4144
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) N-bromosuccinimide; 2.) collidine/xylene / CCl4 / 1.) reflux, 25 min; 2.) reflux, 20 min
2: 20 percent / 5percent potassium hydroxyde / tetrahydrofuran / 1 h / Ambient temperature
3: 15 percent / benzene; ethanol / 1.) irrad., 5 min; 2.) reflux, 1 h
With 2,3,5-trimethyl-pyridine; potassium hydroxide; N-Bromosuccinimide; xylene; In tetrahydrofuran; tetrachloromethane; ethanol; benzene;
DOI:10.1248/cpb.36.4144
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