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Technology Process of [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine

[4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine

Base Information
  • Chemical Name:[4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
  • CAS No.:694446-35-0
  • Molecular Formula:C14H20ClN3O
  • Molecular Weight:281.78
  • Hs Code.:
  • Mol file:694446-35-0.mol
[4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine

Synonyms:[4-(4-butyrylpiperazin-1-yl)-3-chlorophenyl]amine;694446-35-0;1-[4-(4-amino-2-chlorophenyl)piperazin-1-yl]butan-1-one;1-(4-(4-Amino-2-chlorophenyl)piperazin-1-yl)butan-1-one;MFCD03999526;AKOS000111173;LS-09179;BB 0245651;CS-0314609;SR-01000267433;A1-07567;SR-01000267433-1;1-[4-(4-Amino-2-chloro-phenyl)-piperazin-1-yl ]-butan-1-one

Suppliers and Price of [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
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
  • Matrix Scientific
  • [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
  • 1g
  • $ 325.00
  • Biosynth Carbosynth
  • [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
  • 500 mg
  • $ 100.00
  • Biosynth Carbosynth
  • [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
  • 1 g
  • $ 170.00
  • AK Scientific
  • [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
  • 250mg
  • $ 127.00
  • A1 Biochem Labs
  • [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine 95%
  • 5 g
  • $ 700.00
Total 3 raw suppliers
Chemical Property of [4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine
Chemical Property:
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:281.1294900
  • Heavy Atom Count:19
  • Complexity:305
Purity/Quality:

99% *data from raw suppliers

[4-(4-Butyrylpiperazin-1-yl)-3-chlorophenyl]amine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCCC(=O)N1CCN(CC1)C2=C(C=C(C=C2)N)Cl
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