Cas no 276872-81-2 (1-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)methyl]-,1,1-dimethylethyl ester)
![1-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)methyl]-,1,1-dimethylethyl ester structure](https://ossimg.kuujia.com/scimg/277000/276872-81-2x500.png)
276872-81-2 structure
Product Name:1-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)methyl]-,1,1-dimethylethyl ester
CAS No:276872-81-2
MF:C17H24FNO2
MW:293.376368522644
CID:1432619
PubChem ID:22676679
Update Time:2025-04-20
1-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)methyl]-,1,1-dimethylethyl ester Chemical and Physical Properties
Names and Identifiers
-
- 1-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)methyl]-,1,1-dimethylethyl ester
- 4-(4-FLUORO-BENZYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
- tert-butyl 4-[(4-fluorophenyl)methyl]piperidine-1-carboxylate
- SCHEMBL4773466
- GHMYVSNELKFYHM-UHFFFAOYSA-N
- 1-tert-butoxycarbonyl-4-(4-fluorobenzyl)piperidine
- 276872-81-2
- AB72048
- 4-[(4-fluorophenyl)methyl]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester
- 4-(4-Fluoro-benzyl)-1-boc-piperidine
- DB-097062
- N-(t-butoxycarbonyl)-4-(4-fluorophenylmethyl)piperidine
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- Inchi： 1S/C17H24FNO2/c1-17(2,3)21-16(20)19-10-8-14(9-11-19)12-13-4-6-15(18)7-5-13/h4-7,14H,8-12H2,1-3H3
- InChI Key： GHMYVSNELKFYHM-UHFFFAOYSA-N
- SMILES： FC1C=CC(=CC=1)CC1CCN(C(=O)OC(C)(C)C)CC1
Computed Properties
- Exact Mass: 293.17922
- Monoisotopic Mass: 293.17910717g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 21
- Rotatable Bond Count: 4
- Complexity: 337
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.9
- Topological Polar Surface Area: 29.5?2
Experimental Properties
- PSA: 29.54
1-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)methyl]-,1,1-dimethylethyl ester Related Literature
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283
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Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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