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13406-98-9 (哌啶-1-羧酸,piperidine-1-carboxylic acid)

结构式：

哌啶-1-羧酸结构式图片|13406-98-9结构式图片

哌啶-1-羧酸MOL文件

CAS号：

13406-98-9

中文名称：

哌啶-1-羧酸

英文名称：

piperidine-1-carboxylic acid

分子式：

C₆H₁₁NO₂

分子量：

129.15704

相关分类：

溶剂及有机化学品 > 有机化合物 > Organoheterocyclic compounds > Piperidines > Piperidinecarboxylic acids and derivatives > Piperidinecarboxylic acids

溶剂及有机化学品 > 有机化合物 > Organoheterocyclic compounds > Piperidines > Piperidinecarboxylic acids

哌啶-1-羧酸(13406-98-9)名称与标识符

名称

中文别名：

哌啶-1-羧酸;

英文别名：

1-Piperidinecarboxylic acid;Piperidine-1-carboxylic acid;1-Carbamylpiperidine;1-Piperidinecarboxamide;2S-piperidinecarboxylic acid;4-piperidylcarboxylic acid;D,L-piperidinecarboxylic acid;dihydropyridine amide;dihydropyridinemonocarboxylic acid;L-piperidin-2-ylcarboxylic acid;N,N-Pentamethyleneurea;N-carbamoylpiperidine;piperidine carboxamide;piperidine carboxylic acid ester;piperidine-amide;Piperidine-N-carbonic acid amide;piperidino carboxami;piperidylcarboxamide;PIPERIDINE-CARBOXYLIC ACID;

标识符

InChIKey：

DNUTZBZXLPWRJG-UHFFFAOYSA-N

Inchi：

InChI=1S/C6H11NO2/c8-6(9)7-4-2-1-3-5-7/h1-5H2,(H,8,9)

SMILES：

C1CCN(CC1)C(=O)O

哌啶-1-羧酸(13406-98-9)物化性质

实验特性

LogP : 1.08820
PSA : 40.54000

计算特性

精确分子量 : 129.07900
氢键供体数量 : 1
氢键受体数量 : 3
可旋转化学键数量 : 1
重原子数量 : 9

哌啶-1-羧酸(13406-98-9)相关文献

1. Proton transfer in intramolecular hydrogen bonds with large proton polarizability in 1-piperidinecarboxylic acids. Temperature, solvent and concentration dependence
Rainer Kr?mer,Rudolph Lang,Bogumil Brzezinski,Georg Zundel J. Chem. Soc. Faraday Trans. 1990 86 627
2. Back matter
J. Chem. Soc. Faraday Trans. 1990 86 P325
3. Synthesis of the tricyclic core of manzamine A
Ravindra B. Pathak,Benjamin C. Dobson,Nandita Ghosh,Khalid A. Ageel,Madeha R. Alshawish,Rungroj Saruengkhanphasit,Iain Coldham Org. Biomol. Chem. 2015 13 3331
4. Iodonium ylides for one-step, no-carrier-added radiofluorination of electron rich arenes, exemplified with 4-(([18F]fluorophenoxy)-phenylmethyl)piperidine NET and SERT ligands
Jens Cardinale,Johannes Ermert,Sven Humpert,Heinz H. Coenen RSC Adv. 2014 4 17293
5. Asymmetrized tris(hydroxymethyl)methane as a precursor of N- and O-containing 6-membered heterocycles through ring-closing metathesis
Luca Banfi,Giuseppe Guanti,Monica Paravidino,Renata Riva Org. Biomol. Chem. 2005 3 1729
6. Asymmetrized tris(hydroxymethyl)methane as a precursor of N- and O-containing 6-membered heterocycles through ring-closing metathesis
Luca Banfi,Giuseppe Guanti,Monica Paravidino,Renata Riva Org. Biomol. Chem. 2005 3 1729
7. Identification of false positives in “HTS hits to lead”: The application of Bayesian models in HTS triage to rapidly deliver a series of selective TRPV4 antagonists
Sarah E. Skerratt,James E. J. Mills,Jayesh Mistry Med. Chem. Commun. 2013 4 244
8. Contents pages
J. Chem. Soc. Faraday Trans. 1990 86 P041
9. Synthesis and derivatisation of a novel spiro[1-benzofuran-2,4′-piperidin]-3-one scaffold
Rowan A. Wilson,Lai Chan,Robin Wood,Richard C. D. Brown Org. Biomol. Chem. 2005 3 3228
10. Zinc(ii)-mediated generation of 5-amino substituted 2,3-dihydro-1,2,4-oxadiazoles and their further ZnII-catalyzed and O2-involving transformations
Andrey S. Smirnov,Ekaterina S. Yandanova,Nadezhda A. Bokach,Galina L. Starova,Vladislav V. Gurzhiy,Margarita S. Avdontceva,Andrey A. Zolotarev,Vadim Yu. Kukushkin New J. Chem. 2015 39 9330

目录

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相关产品厂家

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问答

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