1,3-aminoalcohols
1,3-Aminoalcohols are a class of organic compounds characterized by the presence of both amino (-NH?) and hydroxyl (-OH) functional groups attached to an alcohol group. These molecules are important in various chemical applications due to their unique reactivity profiles. They often serve as precursors in synthesis reactions, acting as chiral auxiliaries or intermediates. In pharmaceuticals, 1,3-aminoalcohols can be used in the development of drug candidates due to their ability to participate in complex molecular interactions and facilitate targeted binding. Additionally, these compounds have applications in materials science, where they can contribute to the formation of specific structures through hydrogen bonding and other intermolecular forces. Their versatile properties make 1,3-aminoalcohols valuable reagents in both academic research and industrial settings.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Phytosphingosine | 554-62-1 | C18H39NO3 |
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1,3,4-Octadecanetriol,2-amino- | 13552-11-9 | C18H39NO3 |
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Zeamine; N1-Deacyl | 1226515-91-8 | C40H87N5O |
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N-(4,5-Diamino-2-hydroxypentanoyl)leucinamide | 1529816-89-4 | C11H24N4O3 |
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3-Tetracontanol, 1,11,19,27,35-pentaamino- | 187844-18-4 | C40H87N5O |
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1,4-Diamino-2-butanol | 13094-22-9 | C4H12N2O |
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1,4-Diamino-2-butanol-(S)-form | 24177-21-7 | C4H12N2O |
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1,4-diaminobutan-2-ol | 539-59-3 | C4H12N2O |
Related Literature
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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