Secondary amines
Secondary amines, also known as N-substituted amines, are organic compounds characterized by having two alkyl or aryl groups attached to the nitrogen atom. These functional groups play a crucial role in various chemical reactions due to their basic nature, which arises from the lone pair of electrons on the nitrogen atom. Secondary amines can be synthesized through various methods such as alkylation of primary amines or reduction of nitriles. They are widely used in organic synthesis, pharmaceuticals, and surfactants. The versatility of secondary amines makes them valuable intermediates for the production of dyestuffs, pesticides, and plasticizers. Their properties can be further modified by introducing different substituents to tailor their reactivity and solubility for specific applications.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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(3-methylbutyl)(propan-2-yl)amine | 56368-82-2 | C8H19N |
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Thiazolo[5,4-b]pyridin-2-amine, N-ethyl- | 62638-69-1 | C8H9N3S |
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1-Oxa-4,10,16-trithia-7,13-diazacyclooctadecane(9CI) | 343372-28-1 | C12H26N2OS3 |
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1,2-Ethanediamine,N1-(2-aminoethyl)-N2-methyl- | 34066-95-0 | C5H15N3 |
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N-Methyladamantan-1-amine | 3717-38-2 | C11H19N |
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Propylbeta-D-glucopyranoside | 34384-77-5 | C9H18O6 |
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1,2-Ethanediamine,N1-(2-methylpropyl)- | 3437-23-8 | C6H16N2 |
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1,2-Ethanediamine,N1-(2-aminoethyl)-N2-octadecyl- | 7261-63-4 | C22H49N3 |
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N-(cyclopropylmethyl)cyclopentanamine | 898911-74-5 | C9H17N |
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2H-Pyrido[3,2-b]-1,4-oxazine,3,4-dihydro-8-methyl- | 801179-01-1 | C8H10N2O |
Related Literature
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
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Raheleh Torabi,Hedayatollah Ghourchian,Massoud Amanlou Org. Biomol. Chem., 2016,14, 8141-8153
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Hailing Chen,Lu Yin,Meng Liu,Laibing Wang,Michiya Fujiki,Wei Zhang RSC Adv., 2019,9, 4849-4856
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