3416-93-1 (2-(4,5-dihydro-1,3-oxazol-2-yl)aniline,2-(4,5-Dihydrooxazol-2-yl)aniline)

快速询单

结构式：

2-(4,5-dihydro-1,3-oxazol-2-yl)anilineMOL文件

CAS号：

3416-93-1

中文名称：

2-(4,5-dihydro-1,3-oxazol-2-yl)aniline

英文名称：

2-(4,5-Dihydrooxazol-2-yl)aniline

分子式：

C₉H₁₀N₂O

分子量：

162.188501834869

2-(4,5-dihydro-1,3-oxazol-2-yl)aniline(3416-93-1)名称与标识符

名称

中文别名：

2-(4,5-dihydro-1,3-oxazol-2-yl)aniline;

英文别名：

2-(4,5-dihydro-1,3-oxazol-2-yl)aniline;2-(2'-anilinyl)-2-oxazoline;BEN354;2-(4,5-dihydrooxazol-2-yl)aniline;Benzenamine, 2-(4,5-dihydro-2-oxazolyl)-;2-(4,5-Dihydro-oxazol-2-yl)-anilin;SureCN7452092;2-(4,5-dihydro-oxazol-2-yl)-aniline;2-(2-Aminophenyl)-2-oxazolin;5-(2-Aminophenyl)-2-oxazolin;2-(2'-anilinyl)-2-oxazoline; BEN354; 2-(4,5-dihydrooxazol-2-yl)aniline; Benzenamine, 2-(4,5-dihydro-2-oxazolyl)-; 2-(4,5-Dihydro-oxazol-2-yl)-anilin; SureCN7452092; 2-(4,5-dihydro-oxazol-2-yl)-aniline; 2-(2-Aminophenyl)-2-oxazolin; 5-(2-Aminophenyl)-2-oxazolin;;2-(o-aminophenyl)oxazoline;SCHEMBL7452092;2-(4,5-Dihydro-2-oxazolyl)benzenamine;AKOS022532978;MFCD18206196;AS-44520;DTXSID10443646;3416-93-1;

标识符

MDL：

MFCD18206196

InChIKey：

FDLSEUGNQNFTFX-UHFFFAOYSA-N

Inchi：

1S/C9H10N2O/c10-8-4-2-1-3-7(8)9-11-5-6-12-9/h1-4H,5-6,10H2

SMILES：

O1CCN=C1C1C=CC=CC=1N

2-(4,5-dihydro-1,3-oxazol-2-yl)aniline(3416-93-1)物化性质

实验特性

PSA : 47.61

计算特性

精确分子量 : 162.0794
氢键供体数量 : 1
氢键受体数量 : 3
可旋转化学键数量 : 1
同位素质量 : 162.079312947g/mol
重原子数量 : 12
复杂度 : 191
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 : 47.6Å²

2-(4,5-dihydro-1,3-oxazol-2-yl)aniline(3416-93-1)相关文献

1. Achiral and chiral NNN-pincer nickel complexes with oxazolinyl backbones: application in transfer hydrogenation of ketones
Rahul A. Jagtap,Shidheshwar B. Ankade,Rajesh G. Gonnade,Benudhar Punji New J. Chem. 2021 45 11927
2. Lewis-acid-promoted cyclization reaction: synthesis of N3-chloroethyl and N3-thiocyanatoethyl quinazolinones
Fang-Peng Hu,Ming-Ming Zhang,Guo-Sheng Huang New J. Chem. 2021 45 9315
3. Clay catalyzed conversion of isatoic anhydride to 2-(o-aminophenyl)oxazolines
Anil S. Gajare,Nadim S. Shaikh,Gowda K. Jnaneshwara,Vishnu H. Deshpande,Thottappilli Ravindranathan,Ashutosh V. Bedekar J. Chem. Soc. Perkin Trans. 1 2000 999
4. Supramolecular ensemble of PBI derivative and copper nanoparticles: a light harvesting antenna for photocatalytic C(sp2)–H functionalization
Sandeep Kaur,Manoj Kumar,Vandana Bhalla Green Chem. 2016 18 5870
5. Comproportionation and disproportionation in nickel and copper complexes
Craig S. Day,Ruben Martin Chem. Soc. Rev. 2023 52 6601
6. Recent advances in cobalt-catalyzed allylic functionalization
Jun-Fa Han,Peng Guo,Xiang-Gui Zhang,Jia-Bin Liao,Ke-Yin Ye Org. Biomol. Chem. 2020 18 7740
7. Base-promoted Lewis acid catalyzed synthesis of quinazoline derivatives
Fang-Peng Hu,Xin-Feng Cui,Guo-Qiang Lu,Guo-Sheng Huang Org. Biomol. Chem. 2020 18 4376
8. Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
Soham Maity,Pravas Dolui,Rajesh Kancherla,Debabrata Maiti Chem. Sci. 2017 8 5181

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问答

实验需要4-(4,5-DIHYDRO-1,3-OXAZOL-2-YL)ANILINE 54472-46-7

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