4-氨基-2,2,6,6-四甲基-4-哌啶是一種有機化合物,化學式為 H2NCH(CH2C(CH3)2)2NH。它被歸類為二胺,為無色油狀液體。
Quick Facts 4-氨基-2,2,6,6-四甲基哌啶, 識別 ...
4-氨基-2,2,6,6-四甲基哌啶
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IUPAC名 2,2,6,6-Tetramethylpiperidin-4-amine 2,2,6,6-四甲基哌啶-4-胺
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別名
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2,2,6,6-四甲基-4-氨基哌啶 4-氨基-2,2,6,6-四甲基哌啶
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識別
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CAS號
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36768-62-4
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PubChem
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37524
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ChemSpider
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34423
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SMILES
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性質
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化學式
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C9H20N2
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摩爾質量
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156.27 g·mol−1
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外觀
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無色液體
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密度
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0.8966 g/cm3
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熔點
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17 °C(290 K)
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沸點
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188.5 °C(462 K)
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危險性
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GHS危險性符號
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GHS提示詞
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危險
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H-術語
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H290, H302, H314, H318, H412
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P-術語
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P234, P260, P264, P270, P273, P280, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P330
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若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。
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該化合物是製備博比特鹽的中間體,博比特鹽是一種用於有機合成的氧化劑。它是由相應酮的還原胺化反應製備的:[1]
- OC(CH2C(CH3)2)2NH + NH3 + H2 → H2NCH(CH2C(CH3)2)2NH + H2O
特魯達(Truda)等人的一項研究報告了大鼠的半數致死量LD(50)為906mg/kg。[2]
- 1,2,2,6,6-五甲基哌啶
- 2,2,6,6-四甲基哌啶
Nabyl Merbouh; James M. Bobbitt; Christian Brückner. Preparation of Tetramethylpiperdine-1-oxoammonlum Salts and Their Use as Oxidants in Organic Chemistry. A Review. Organic Preparations and Procedures International. 2004, 36: 1–31. S2CID 98117103. doi:10.1080/00304940409355369.
[ Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 28(5), Pg. 53, 1984]
- C. McFarland; D. Vicic; A. Debnath. Rapid Microwave-Assisted Syntheses of Derivatives of HIV-1 Entry Inhibitors. Synthesis. 2006, 2006 (5): 807–812. doi:10.1055/s-2006-926339.
- L. Tilley; J. Bobbitt; S. Murray; C. Camire. A Revised Preparation of (4-Acetamido-2,2,6,6-tetramethylpiperidin-1-yl)oxyl and 4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium Tetrafluoroborate: Reagents for Stoichiometric Oxidations of Alcohols. Synthesis. 2013, 45 (3): 326–329. doi:10.1055/s-0032-1317861.
- A. Germanova; L. Aizvert; A. Shidlovskaia; L. Melnikova; M. Bidevkina. Comparative characteristics of the toxicity, safety and nature of the biological effect on the body of 4-hydroxy-2,2,6,6-tetramethylpiperidine and 4-amino-2,2,6,6-tetramethylpiperidine. Gig Tr Prof Zabol. 1984, (5): 53–54. PMID 6745687.
- M. Gergely; A. Takacs; L.Kollar. 4-Amino-TEMPO as N-Nucleophile in Palladium-Catalyzed Aminocarbonylation. Heterocyclic Chemistry. 2016, 54 (1): 634–640. doi:10.1002/jhet.2635.