Benzyl cyanides
Benzyl cyanides are derivatives of benzaldehyde with a cyano group (-CN) attached to the benzylic position. These compounds exhibit a variety of structural and functional properties, making them valuable in both academic research and industrial applications. Structurally, they can be linear or cyclic depending on the specific substituents present. Benzyl cyanides are often used as intermediates in organic synthesis due to their reactivity and versatility.
Their unique chemical behavior arises from the presence of both an electron-donating hydroxymethyl group and an electron-withdrawing cyano group, leading to interesting electronic effects that influence their reactivity and stability. In the pharmaceutical industry, benzyl cyanides have been utilized in the synthesis of various drugs due to their ability to form stable derivatives with biological activity.
These compounds are also important in the production of dyes, pesticides, and fragrances owing to their aromatic nature and ease of functionalization. Additionally, their cytotoxic properties make them useful as research tools in studying cellular mechanisms and potential therapeutic targets.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2-(2-fluoro-4-methylphenyl)acetonitrile | 518070-26-3 | C9H8FN |
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2-(2,6-dimethylphenyl)acetonitrile | 54708-14-4 | C10H11N |
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2-(Trifluoromethylthio)phenylacetonitrile | 237424-20-3 | C9H6F3NS |
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3-Cyanomethylphenylboronic Acid | 220616-39-7 | C8H8BNO2 |
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2-(3,4-Dimethylphenyl)acetonitrile | 3020-06-2 | C10H11N |
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2-3-(difluoromethoxy)phenylacetonitrile | 41429-18-9 | C9H7F2NO |
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Benzeneacetonitrile,3(or 4)-ethenyl- (9CI) | 110013-89-3 | C10H9N |
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O4I1 | 175135-47-4 | C16H15NO2 |
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2-(4-(3,4-Dichlorobenzyl)OxyPhenyl)Acetonitrile | 175135-34-9 | C15H11Cl2NO |
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(4-Hydrazinophenyl)acetonitrile | 57411-91-3 | C8H9N3 |
Related Literature
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Felix Witte,Philipp Rietsch,Nithiya Nirmalananthan-Budau,Florian Weigert,Jan P. G?tze,Ute Resch-Genger,Siegfried Eigler,Beate Paulus Phys. Chem. Chem. Phys., 2021,23, 17521-17529
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Xin Li,Liangliang Zhu,Sai Duan,Yanli Zhao,Hans ?gren Phys. Chem. Chem. Phys., 2014,16, 23854-23860
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Nduka Ikpo,Jenna C. Flogeras,Francesca M. Kerton Dalton Trans., 2013,42, 8998-9006
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Kui Wu,Zhihua Yang,Shilie Pan Dalton Trans., 2015,44, 19856-19864
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Hyejin Moon,Aaron R. Wheeler,Robin L. Garrell,Chang-Jin “CJ” Kim Lab Chip, 2006,6, 1213-1219
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