Cas no 109732-23-2 (1-Piperidinepropanamide,N-(1-phenylethyl)-, hydrochloride (1:1))
109732-23-2 structure
Product Name:1-Piperidinepropanamide,N-(1-phenylethyl)-, hydrochloride (1:1)
CAS No:109732-23-2
MF:C16H25ClN2O
MW:296.835503339767
CID:210579
PubChem ID:3066194
Update Time:2025-04-19
1-Piperidinepropanamide,N-(1-phenylethyl)-, hydrochloride (1:1) Chemical and Physical Properties
Names and Identifiers
-
- 1-Piperidinepropanamide,N-(1-phenylethyl)-, hydrochloride (1:1)
- 1-Piperidinepropionamide,N-a-methylbenzyl-, hydrochloride(6CI)
- N-benzyl-N-methyl-3-piperidin-1-ylpropanamide,hydrochloride
- N-(alpha-Phenylaethyl)-beta-piperidinopropionsaeureamid-hydrochlorid
- DTXSID40149023
- 109732-23-2
- N-(alpha-Phenylaethyl)-beta-piperidinopropionsaeureamid-hydrochlorid [German]
- 1-Piperidinepropionamide, N-(alpha-methylbenzyl)-, hydrochloride
- N-(alpha-Methylbenzyl)-1-piperidinepropionamide hydrochloride
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- Inchi： 1S/C16H24N2O.ClH/c1-17(14-15-8-4-2-5-9-15)16(19)10-13-18-11-6-3-7-12-18;/h2,4-5,8-9H,3,6-7,10-14H2,1H3;1H
- InChI Key： JEGOWWKQIDCXHY-UHFFFAOYSA-N
- SMILES： Cl.O=C(CCN1CCCCC1)N(C)CC1C=CC=CC=1
Computed Properties
- Exact Mass: 296.16575
- Monoisotopic Mass: 296.166
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 20
- Rotatable Bond Count: 5
- Complexity: 268
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 23.6?2
Experimental Properties
- Boiling Point: 409°C at 760 mmHg
- Flash Point: 171.7°C
- PSA: 23.55
- LogP: 3.26090
1-Piperidinepropanamide,N-(1-phenylethyl)-, hydrochloride (1:1) Related Literature
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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Vitaly Gurylev,Chung-Yi Su,Tsong-Pyng Perng Phys. Chem. Chem. Phys., 2016,18, 16033-16038
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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