13115-24-7 ((N-hydroxy-N-methylacetamide)

快速询单

结构式：

N-hydroxy-N-methylacetamideMOL文件

CAS号：

13115-24-7

英文名称：

N-hydroxy-N-methylacetamide

分子式：

C₃H₇NO₂

分子量：

89.0931808948517

N-hydroxy-N-methylacetamide(13115-24-7)名称与标识符

名称

英文别名：

Acetamide,N-hydroxy-N-methyl-;N-hydroxy-N-methylacetamide;N-methyl acetohydroxamic acid;ACETOHYDROXAMIC ACID, N-METHYL-;AI3-61934;N-Acetyl-N-methylhydroxylamine;N-hydroxy-N-methyl-acetamide;N-methyacetylhydroxamic acid;N-methyl-acetohydroxamic acid;N-Methylacetohydroxamic acid;NMAH acid;NSC-329234;N-METHYL-N-ACETYLHYDROXYLAMINE;Acetamide, N-hydroxy-N-methyl-;CHEMBL4761573;7BXE337G7T;UNII-7BXE337G7T;EN300-261005;NSC 329234;NoName_1668;AKOS006273714;NSC329234;DTXSID10902425;13115-24-7;

标识符

MDL：

MFCD00912835

InChIKey：

BJPJMTMWIVUMAK-UHFFFAOYSA-N

Inchi：

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

SMILES：

ON(C)C(C)=O

N-hydroxy-N-methylacetamide(13115-24-7)物化性质

实验特性

LogP : -0.14610
PSA : 40.54

计算特性

精确分子量 : 89.04771
氢键供体数量 : 1
氢键受体数量 : 2
可旋转化学键数量 : 0
同位素质量 : 89.047678466g/mol
重原子数量 : 6
复杂度 : 61.8
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） : -0.8
拓扑分子极性表面积 : 40.5Å²

N-hydroxy-N-methylacetamide(13115-24-7)相关文献

1. Novel half-sandwich Ru(II)-hydroxamate complexes: synthesis, characterization and equilibrium study in aqueous solution
Péter Buglyó,Etelka Farkas Dalton Trans. 2009 8063
2. Siderophore analogues. Synthesis and chelating properties of a new macrocyclic trishydroxamate ligand
M. Alexandra Esteves,M. Candida T. Vaz,M. L. S. Sim?es Gon?alves,Etelka Farkas,M. Amélia Santos J. Chem. Soc. Dalton Trans. 1995 2565
3. A newly designed heterodiene and its application to construct six-membered heterocycles containing an N–O bond
Wenzhi Ji,Chen-Long Li,Hui Chen,Zhi-Xiang Yu,Xuebin Liao Chem. Commun. 2019 55 12012
4. Conformational behavior of some hydroxamic acids
Rita Kakkar,Rajni Grover,Preeti Chadha Org. Biomol. Chem. 2003 1 2200
5. Microscopic acid–base equilibria of a synthetic hydroxamate siderophore analog, piperazine-1,4-bis(N-methylacetohydroxamic acid)
M. Amélia Santos,M. Alexandra Esteves,M. Candida Vaz,J. J. R. Fraústo da Silva,Bela Noszal,Etelka Farkas J. Chem. Soc. Perkin Trans. 2 1997 1977
6. Microscopic acid–base equilibria of a synthetic hydroxamate siderophore analog, piperazine-1,4-bis(N-methylacetohydroxamic acid)
M. Amélia Santos,M. Alexandra Esteves,M. Candida Vaz,J. J. R. Fraústo da Silva,Bela Noszal,Etelka Farkas J. Chem. Soc. Perkin Trans. 2 1997 1977
7. The kinetics of dimethylhydroxypyridinone interactions with iron(iii) and the catalysis of iron(iii) ligand exchange reactions: implications for bacterial iron transport and combination chelation therapies
James M. Harrington,Manu M. Mysore,Alvin L. Crumbliss Dalton Trans. 2018 47 6954
8. Siderophore analogues: a new macrocyclic tetraamine tris(hydroxamate) ligand; synthesis and solution chemistry of the iron(III), aluminium(III) and copper(II) complexes??
Margarida Gaspar,Raquel Grazina,Andrea Bodor,Etelka Farkas,M. Amélia Santos J. Chem. Soc. Dalton Trans. 1999 799
9. Modeling the inhibition of peptide deformylase by hydroxamic acids: influence of the sulfur donor
Erwan Galardon,Michel Giorgi,Isabelle Artaud Dalton Trans. 2007 1047
10. Charting the mechanism and reactivity of zirconium oxalate with hydroxamate ligands using density functional theory: implications in new chelate design
Jason P. Holland,Neil Vasdev Dalton Trans. 2014 43 9872

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