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1-(2-Cyclohexylethyl)piperazine

Base Information Edit
  • Chemical Name:1-(2-Cyclohexylethyl)piperazine
  • CAS No.:132800-12-5
  • Molecular Formula:C12H24 N2
  • Molecular Weight:196.33
  • Hs Code.:2933599090
  • European Community (EC) Number:671-069-8
  • DSSTox Substance ID:DTXSID00370997
  • Wikidata:Q82158201
  • Mol file:132800-12-5.mol
1-(2-Cyclohexylethyl)piperazine

Synonyms:1-(2-cyclohexylethyl)piperazine;132800-12-5;Piperazine,1-(2-cyclohexylethyl)-;SCHEMBL1623678;DTXSID00370997;MFCD01320901;AKOS009157743;AS-44262;1-(2-Cyclohexylethyl)piperazine, AldrichCPR;CS-0271623;FT-0750096;EN300-898383;A806500

Suppliers and Price of 1-(2-Cyclohexylethyl)piperazine
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
  • SynQuest Laboratories
  • 1-(2-Cyclohexylethyl)piperazine 97%
  • 5 g
  • $ 248.00
  • SynQuest Laboratories
  • 1-(2-Cyclohexylethyl)piperazine 97%
  • 25 g
  • $ 376.00
  • Crysdot
  • 1-(2-Cyclohexylethyl)piperazine 95+%
  • 5g
  • $ 353.00
  • American Custom Chemicals Corporation
  • 1-(2-CYCLOHEXYLETHYL)PIPERAZINE 95.00%
  • 10G
  • $ 1304.36
  • American Custom Chemicals Corporation
  • 1-(2-CYCLOHEXYLETHYL)PIPERAZINE 95.00%
  • 5G
  • $ 907.92
  • American Custom Chemicals Corporation
  • 1-(2-CYCLOHEXYLETHYL)PIPERAZINE 95.00%
  • 1G
  • $ 613.88
Total 8 raw suppliers
Chemical Property of 1-(2-Cyclohexylethyl)piperazine Edit
Chemical Property:
  • Boiling Point:98-100°C/0.5 mm 
  • PSA:15.27000 
  • LogP:2.12870 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:196.193948774
  • Heavy Atom Count:14
  • Complexity:146
Purity/Quality:

98% *data from raw suppliers

1-(2-Cyclohexylethyl)piperazine 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CCC(CC1)CCN2CCNCC2
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