{{Chembox | ImageFile = Cyclopentylamine.svg | ImageSize = | ImageAlt = | IUPACName = | OtherNames = aminocyclopentane |Section1={{Chembox Identifiers | CASNo = 1003-03-8 | CASNo_Ref = {{Cascite|correct|CAS}} | ChEMBL = 1171859 | ChemSpiderID = 2803 | EC_number = 213-697-3 | PubChem = 2906 | UNII = 4259VRY3GN | StdInChI=1S/C5H11N/c6-5-3-1-2-4-5/h5H,1-4,6H2 | StdInChIKey = NISGSNTVMOOSJQ-UHFFFAOYSA-N | SMILES = C1CCC(C1)N }} |Section2={{Chembox Properties | C = 5|N = 1|H=11 | MolarMass = | RefractIndex = | Appearance = colorless liquid | Density = 0.8512 g/cm<sup>3</sup> | MeltingPtC = -82.7 | MeltingPt_notes = | BoilingPtC = 106-8 | BoilingPt_notes = 750 Torr | pKa = 10.65 (conjugate acid) | Solubility = }} |Section3={{Chembox Hazards | GHS_ref=[https://pubchem.ncbi.nlm.nih.gov/compound/2906#section=Safety-and-Hazards] | GHSPictograms = {{GHS02}}{{GHS05}}{{GHS06}}{{GHS07}} | GHSSignalWord = Danger | HPhrases = {{H-phrases|225|300|314|315|317|331|332|412}} | PPhrases = {{P-phrases|210|233|240|241|242|243|260|261|264|264+265|270|271|272|273|280|301+316|301+330+331|302+352|302+361+354|303+361+353|304+340|305+354+338|316|317|321|330|332+317|333+317|362+364|363|370+378|403+233|403+235|405|501}} | MainHazards = | FlashPt = | AutoignitionPt = }} }}
'''Cyclopentylamine''' is an organic compound with the formula {{chem2|C5H9NH2}}. It is a colorless, readily distillable liquid. Cyclopentylamine is a member of the aminocycloalkanes, which also includes cyclopropylamine, cyclobutylamine, and cyclohexylamine.
Cyclopentylamine can be prepared by reductive amination starting with cyclopentanone or cyclopentanol.<ref>{{cite journal |last1=Pingen |first1=Dennis |last2=Müller |first2=Christian |last3=Vogt |first3=Dieter |title=Direct Amination of Secondary Alcohols Using Ammonia |journal=Angewandte Chemie International Edition |date=2010 |volume=49 |issue=44 |pages=8130–8133 |doi=10.1002/anie.201002583 |pmid=20672264 |bibcode=2010ACIE...49.8130P }}</ref> ==References== <references />
{{Commonscat}}
Category:Amines Category:Cyclopentyl compounds
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