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N-(sec-Butyl)-4-piperidinecarboxamide hydrochloride

Base Information Edit
  • Chemical Name:N-(sec-Butyl)-4-piperidinecarboxamide hydrochloride
  • CAS No.:1220027-92-8
  • Molecular Formula:C10H21ClN2O
  • Molecular Weight:220.74
  • Hs Code.:
  • Mol file:1220027-92-8.mol
N-(sec-Butyl)-4-piperidinecarboxamide hydrochloride

Synonyms:1220027-92-8;N-(sec-Butyl)-4-piperidinecarboxamide hydrochloride;N-(sec-butyl)piperidine-4-carboxamide hydrochloride;N-butan-2-ylpiperidine-4-carboxamide;hydrochloride;N-(sec-Butyl)-4-piperidinecarboxamidehydrochloride;AKOS015847091;N-(sec-butyl)piperidine-4-carboxamidehydrochloride;N-(butan-2-yl)piperidine-4-carboxamide hydrochloride

Suppliers and Price of N-(sec-Butyl)-4-piperidinecarboxamide hydrochloride
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
  • Matrix Scientific
  • N-(sec-Butyl)-4-piperidinecarboxamidehydrochloride
  • 500mg
  • $ 237.00
  • Matrix Scientific
  • N-(sec-Butyl)-4-piperidinecarboxamidehydrochloride
  • 2.500g
  • $ 720.00
  • Crysdot
  • N-(sec-Butyl)piperidine-4-carboxamidehydrochloride 95+%
  • 5g
  • $ 446.00
  • American Custom Chemicals Corporation
  • N-(SEC-BUTYL)-4-PIPERIDINECARBOXAMIDE HYDROCHLORIDE 95.00%
  • 2.5G
  • $ 1468.50
  • American Custom Chemicals Corporation
  • N-(SEC-BUTYL)-4-PIPERIDINECARBOXAMIDE HYDROCHLORIDE 95.00%
  • 500MG
  • $ 837.38
Total 1 raw suppliers
Chemical Property of N-(sec-Butyl)-4-piperidinecarboxamide hydrochloride Edit
Chemical Property:
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:220.1342410
  • Heavy Atom Count:14
  • Complexity:164
Purity/Quality:

98%min *data from raw suppliers

N-(sec-Butyl)-4-piperidinecarboxamidehydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC(C)NC(=O)C1CCNCC1.Cl
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