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Technology Process of Methimepip dihydrobromide

Methimepip dihydrobromide

Base Information
  • Chemical Name:Methimepip dihydrobromide
  • CAS No.:817636-54-7
  • Molecular Formula:C10H17N3.2BrH
  • Molecular Weight:260.17400
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80462102
  • Wikipedia:Methimepip
  • Mol file:817636-54-7.mol
Methimepip dihydrobromide

Synonyms:Methimepip dihydrobromide;817636-54-7;151070-80-3;Methimepip (hydrobromide);4-(1H-imidazol-5-ylmethyl)-1-methylpiperidine;dihydrobromide;4-((1H-imidazol-4-yl)methyl)-1-methylpiperidine dihydrobromide;4-[(1H-Imidazol-4-yl)methyl]-1-methylpiperidine dihydrobromide;DTXSID80462102;AKOS024457350;AKOS040756007;PD079525;J-008778;Methimepip dihydrobromide|4-(1H-Imidazol-4-ylmethyl)-1-methylpiperidine dihydrobromide

Suppliers and Price of Methimepip dihydrobromide
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
  • Usbiological
  • Methimepip dihydrobromide
  • 10mg
  • $ 438.00
  • TRC
  • 4-(1H-Imidazol-4-ylmethyl)-1-methylpiperidineDihydrobromide
  • 50mg
  • $ 825.00
  • TRC
  • 4-(1H-Imidazol-4-ylmethyl)-1-methylpiperidineDihydrobromide
  • 10mg
  • $ 200.00
Total 2 raw suppliers
Chemical Property of Methimepip dihydrobromide
Chemical Property:
  • Melting Point:156.7-157.3 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7)) 
  • PSA：31.92000 
  • LogP:2.19000 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:340.99252
  • Heavy Atom Count:15
  • Complexity:152
Purity/Quality:

99% *data from raw suppliers

Methimepip dihydrobromide *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1CCC(CC1)CC2=CN=CN2.Br.Br
  • Uses 4-(1H-Imidazol-4-ylmethyl)-1-methylpiperidine Dihydrobromide is a salt analog of methimepip, which exhibits high affinity and agonist activity at the human histamine H3 receptor.
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