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Technology Process of N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride

N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride

Base Information
  • Chemical Name:N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride
  • CAS No.:86683-98-9
  • Molecular Formula:C17H21 N3 O2 . Cl H
  • Molecular Weight:0
  • Hs Code.:
  • DSSTox Substance ID:DTXSID101007018
  • Mol file:86683-98-9.mol
N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride

Synonyms:86683-98-9;N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride;beta-Methyl-N-(3-phenyl-5-isoxazolyl)-1-pyrrolidinepropanamide hydrochloride;1-Pyrrolidinepropanamide, beta-methyl-N-(3-phenyl-5-isoxazolyl)-, monohydrochloride;DTXSID101007018;LS-138115;N-(3-Phenyl-1,2-oxazol-5-yl)-3-(pyrrolidin-1-yl)butanimidic acid--hydrogen chloride (1/1)

Suppliers and Price of N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride
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
  • American Custom Chemicals Corporation
  • 1-PYRROLIDINEPROPANAMIDE, BETA-METHYL-N-(3-PHENYL-5-ISOXAZOLYL)-, MONO HYDROCHLORIDE 95.00%
  • 5MG
  • $ 502.34
Total 0 raw suppliers
Chemical Property of N-(3-Phenyl-5-isoxazolyl)-3-pyrrolidinobutanamide hydrochloride
Chemical Property:
  • Vapor Pressure:1.13E-11mmHg at 25°C 
  • Boiling Point:538.7°C at 760 mmHg 
  • Flash Point:279.6°C 
  • PSA：61.86000 
  • LogP:4.54390 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:335.1400546
  • Heavy Atom Count:23
  • Complexity:365
Purity/Quality:

1-PYRROLIDINEPROPANAMIDE, BETA-METHYL-N-(3-PHENYL-5-ISOXAZOLYL)-, MONO HYDROCHLORIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CC(=O)NC1=CC(=NO1)C2=CC=CC=C2)N3CCCC3.Cl
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