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Dichloroisoproterenol

Base Information Edit
  • Chemical Name:Dichloroisoproterenol
  • CAS No.:59-61-0
  • Molecular Formula:C11H15 Cl2 N O
  • Molecular Weight:248.152
  • Hs Code.:
  • UNII:U7NOE2K4M2
  • DSSTox Substance ID:DTXSID20874225
  • Nikkaji Number:J4.793G
  • Wikipedia:Dichloroisoprenaline
  • Wikidata:Q387276
  • Metabolomics Workbench ID:153721
  • ChEMBL ID:CHEMBL30816
  • Mol file:59-61-0.mol
Dichloroisoproterenol

Synonyms:dichloroisoproterenol;L-20522

Suppliers and Price of Dichloroisoproterenol
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
Total 4 raw suppliers
Chemical Property of Dichloroisoproterenol Edit
Chemical Property:
  • Vapor Pressure:7.67E-06mmHg at 25°C 
  • Refractive Index:1.5490 (estimate) 
  • Boiling Point:361°Cat760mmHg 
  • PKA:13.32±0.20(Predicted) 
  • Flash Point:172.1°C 
  • PSA:72.72000 
  • Density:1.221g/cm3 
  • LogP:2.30390 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:247.0530695
  • Heavy Atom Count:15
  • Complexity:189
Purity/Quality:

98%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)NCC(C1=CC(=C(C=C1)Cl)Cl)O
  • Recent ClinicalTrials:D-chiro-inositol and Endometrial Thickness
Technology Process of Dichloroisoproterenol

There total 3 articles about Dichloroisoproterenol 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:
isopropylamine; 2-(3,4-dichlorophenyl)-2-oxoacetaldehyde; In 1,2-dichloro-ethane; at 25 ℃; for 2h;
With sodium tetrahydroborate; In 1,2-dichloro-ethane; at 0 ℃; for 2h;
Guidance literature:
Multi-step reaction with 2 steps
1: tetrachlorosilane; N,N,N,N,N,N-hexamethylphosphoric triamide / dichloromethane / 4 h / -20 °C / Inert atmosphere
2: ammonia borane / dichloromethane / 3 h / -20 - 20 °C / Inert atmosphere
With N,N,N,N,N,N-hexamethylphosphoric triamide; ammonia borane; tetrachlorosilane; In dichloromethane; 1: |Passerini Condensation;
DOI:10.1002/chem.201500210
Guidance literature:
With ammonia borane; In dichloromethane; at -20 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1002/chem.201500210
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