^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]
延申阅读
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.
行進 25, 2023
氨基, 四甲基哌啶, 氨基, 四甲基, 哌啶是一种有机化合物, 化学式为, h2nch, ch2c, 它被归类为二胺, 为无色油状液体, iupac名2, tetramethylpiperidin, amine2, 四甲基哌啶, 胺别名, 四甲基, 氨基哌啶识别cas号, 36768, 4pubchem, 37524chemspider, 34423smiles, c性质化学式, c9h20n2摩尔质量, 1外观, 无色液体密度, 8966, cm3熔点, 沸点, 危险性ghs危险性符号ghs提示词, 危险h, 术. 4 氨基 2 2 6 6 四甲基 4 哌啶是一种有机化合物 化学式为 H2NCH CH2C CH3 2 2NH 它被归类为二胺 为无色油状液体 4 氨基 2 2 6 6 四甲基哌啶IUPAC名2 2 6 6 Tetramethylpiperidin 4 amine2 2 6 6 四甲基哌啶 4 胺别名 2 2 6 6 四甲基 4 氨基哌啶4 氨基 2 2 6 6 四甲基哌啶识别CAS号 36768 62 4PubChem 37524ChemSpider 34423SMILES CC1 CC CC N1 C C N C性质化学式 C9H20N2摩尔质量 156 27 g mol 1外观 无色液体密度 0 8966 g cm3熔点 17 C 290 K 沸点 188 5 C 462 K 危险性GHS危险性符号GHS提示词 危险H 术语 H290 H302 H314 H318 H412P 术语 P234 P260 P264 P270 P273 P280 P301 312 P301 330 331 P303 361 353 P304 340 P305 351 338 P310 P321 P330若非注明 所有数据均出自标准状态 25 100 kPa 下 该化合物是制备博比特盐的中间体 博比特盐是一种用于有机合成的氧化剂 它是由相应酮的还原胺化反应制备的 1 OC CH2C CH3 2 2NH NH3 H2 H2NCH CH2C CH3 2 2NH H2O目录 1 毒性 2 相关化合物 3 参考资料 4 延申阅读毒性 编辑特鲁达 Truda 等人的一项研究报告了大鼠的半数致死量LD 50 为906mg kg 2 相关化合物 编辑1 2 2 6 6 五甲基哌啶 2 2 6 6 四甲基哌啶参考资料 编辑 Nabyl Merbouh James M Bobbitt Christian Bruckner 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 延申阅读 编辑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 取自 https zh wikipedia org w index php title 4 氨基 2 2 6 6 四甲基哌啶 amp oldid 76330524, 维基百科，wiki，书籍，书籍，图书馆，
