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2580-63-4 ((N-hydroxypropanamide)

结构式：

N-hydroxypropanamide结构式图片|2580-63-4结构式图片

N-hydroxypropanamideMOL文件

CAS号：

2580-63-4

英文名称：

N-hydroxypropanamide

分子式：

C₃H₇NO₂

分子量：

89.0931808948517

相关分类：

溶剂及有机化学品 > 有机化合物 > 有机酸及其衍生物 > 羧酸及其衍生物 > 羧酸衍生物 > 羧酸酰胺

N-hydroxypropanamide(2580-63-4)名称与标识符

名称

英文别名：

Propanamide, N-hydroxy-;N-hydroxypropanamide;N-Hydroxypropionamide;Propiohydroxamic acid;Propionhydroxamic acid;Propionohydroxamic acid;USAF CS-502;PROPIONOHYDROXIMIC ACID;ZAMI-633;AKOS000191131;UNII-9K8TD4EMP0;XGM;PD061922;NS00027971;Q27272667;EN300-211443;EINECS 219-946-2;RSIPQHOWTCNEBI-UHFFFAOYSA-N;9K8TD4EMP0;CHEMBL4303316;2580-63-4;ethyl hydroximic acid;MFCD00154630;DTXSID30180460;

标识符

MDL：

MFCD00154630

InChIKey：

RSIPQHOWTCNEBI-UHFFFAOYSA-N

Inchi：

1S/C3H7NO2/c1-2-3(5)4-6/h6H,2H2,1H3,(H,4,5)

SMILES：

O=C(CC)NO

N-hydroxypropanamide(2580-63-4)物化性质

实验特性

PSA : 49.33
折射率 : 1.431
沸点 : °Cat760mmHg
闪点 : °C
密度 : 1.093

计算特性

精确分子量 : 89.04771
氢键供体数量 : 2
氢键受体数量 : 2
可旋转化学键数量 : 1
同位素质量 : 89.048
重原子数量 : 6
复杂度 : 52.8
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : -0.5
拓扑分子极性表面积 : 49.3A^2

N-hydroxypropanamide(2580-63-4)相关文献

1. Synthesis and antiproliferative assay of triazolyl-2,2-dimethyl-3-phenylpropanoates as potential HDAC inhibitors
Samir El-Rayes,Gomaa M. S.,Abouelmagd A.,Walid Fathalla,Ibrahim. A. I. Ali RSC Adv. 2019 9 13896
2. Thermodynamic and spectrophotometric investigation of complex formation between hydrogen, cobalt(II), nickel(II), and copper(II) ions and 2-amino-N-hydroxypropanamide in aqueous solution
Enrico Leporati J. Chem. Soc. Dalton Trans. 1989 1299
3. Potentiometric study on the complex-formation equilibria between 2-amino-N-hydroxyhexanamide and α-amino-1H-indole-3-N-hydroxypropanamide and cobalt(II), nickel(II), copper(II), and hydrogen ions in aqueous solution
Enrico Leporati J. Chem. Soc. Dalton Trans. 1988 421
4. Discovery of potential anti-inflammatory drugs: diaryl-1,2,4-triazoles bearing N-hydroxyurea moiety as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase
Bo Jiang,Xiaojing Huang,Hequan Yao,Jieyun Jiang,Xiaoming Wu,Siyi Jiang,Qiujuan Wang,Tao Lu,Jinyi Xu Org. Biomol. Chem. 2014 12 2114
5. Interaction of 2-amino-N-hydroxypropanamide with vanadium(V) in aqueous solution
Regina T. Yamaki,Eucler B. Paniago,Sandra Carvalho,Ivana S. Lula J. Chem. Soc. Dalton Trans. 1999 4407
6. Complex-forming properties of L-α-alaninehydroxamic acid (2-amino-N-hydroxypropanamide)
Etelka Farkas,József Sz?ke,Tamás Kiss,Henryk Kozlowski,Wojciech Bal J. Chem. Soc. Dalton Trans. 1989 2247
7. Effects of side chain amino nitrogen donor atoms on metal complexation of aminohydroxamic acids: New diaminohydroxamates chelating Ni(ii) more strongly than Fe(iii)
éva A. Enyedy,Hajnalka Csóka,István Lázár,Giovanni Micera,Eugenio Garribba,Etelka Farkas nitrogen donor atoms on metal complexation of aminohydroxamic acids: New diaminohydroxamates chelating Ni(ii) more strongly than Fe(iii). éva A. Enyedy Hajnalka Csóka István Lázár Giovanni Micera Eugenio Garribba Etelka Farkas J. Chem. Soc. Dalton Trans. 2002 2632
8. Half-sandwich type rhodium(iii)–aminohydroxamate complexes: the role of the position of the amino group in metal ion binding
Péter László Parajdi-Losonczi,Péter Buglyó,Hana Skakalova,Jana Kasparkova,Norbert Lihi,Etelka Farkas New J. Chem. 2018 42 7659
9. A two-step tandem reaction to prepare hydroxamic acids directly from alcohols
Giovanna Dettori,Silvia Gaspa,Andrea Porcheddu,Lidia De Luca Org. Biomol. Chem. 2014 12 4582
10. Nickel nanoparticles: a highly efficient and retrievable catalyst for the solventless Friedlander annulation of quinolines and their in silico molecular docking studies as histone deacetylase inhibitors
Gangadhara Angajala,Radhakrishnan Subashini RSC Adv. 2015 5 45599

目录

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960化工网为您提供N-hydroxypropanamide专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.2580-63-4,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:2580-63-4 国际站:2580-63-4

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