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Magnesium perchlorate

Base Information
  • Chemical Name:Magnesium perchlorate
  • CAS No.:10034-81-8
  • Deprecated CAS:30298-04-5,74913-43-2,1189671-44-0
  • Molecular Formula:ClHO4. 1/2Mg
  • Molecular Weight:223.21
  • Hs Code.:
  • European Community (EC) Number:233-108-3
  • UN Number:1475
  • UNII:7N77Z541YF
  • DSSTox Substance ID:DTXSID70890617
  • Nikkaji Number:J43.886C
  • Wikipedia:Magnesium perchlorate
  • Wikidata:Q417970
  • Mol file:10034-81-8.mol
Magnesium perchlorate

Synonyms:magnesium perchlorate

Suppliers and Price of Magnesium perchlorate
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
Total 14 raw suppliers
Chemical Property of Magnesium perchlorate
Chemical Property:
  • Appearance/Colour:white crystalline powder 
  • Melting Point:251 °C 
  • PSA:148.54000 
  • Density:2.21 g/cm3 
  • LogP:0.42860 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:0
  • Exact Mass:221.8820640
  • Heavy Atom Count:11
  • Complexity:95.8
  • Transport DOT Label:Oxidizer
Purity/Quality:

99.9% *data from raw suppliers

Safty Information:
  • Pictogram(s): OxidizingO, IrritantXi 
  • Hazard Codes:O, Xi 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Perchlorates
  • Canonical SMILES:[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[Mg+2]
Refernces

An expeditious green synthesis of Schiff bases and azetidinones derivatised with 1,2,4-triazoles

10.1007/s12039-011-0138-8

The research focuses on the efficient green synthesis of Schiff bases and azetidinones derivatised with 1,2,4-triazoles. The study employs Mg(ClO4)2 as a catalyst for the synthesis of Schiff bases from 1-amino-2-aryl-3-oxo-1,2,4-triazoles with various aldehydes under solvent-free conditions. The resulting Schiff bases are then reacted with chloroacetyl chloride to yield azetidinones, also in solvent-free conditions, with excellent yields. The synthesized compounds were analyzed for their potential as drugs by evaluating properties such as penetration into biological membranes (clogP), drug-likeliness, and drug scores. Additionally, the compounds were screened for antitubercular and antimicrobial activities. The analyses included techniques such as IR spectroscopy, 1H NMR spectroscopy, mass spectrometry, and elemental analysis, as well as thin layer chromatography (TLC) to check the purity of the compounds. The pharmacological evaluation was carried out at a separate facility, and the OSIRIS property explorer was used for computational drug analysis.

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