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维基百科

樟脑醌

樟脑醌是一种有机化合物,化学式为C10H14O2,它在牙科材料中用作光引发剂。[2]它可由樟脑乙酸中经二氧化硒氧化制得。[3]它可以被次氯酸钠进一步氧化为樟脑酸[4]它的两个羰基(C=O)也能被氢化铝锂还原为羟基(C-OH)。[5]

樟脑醌
IUPAC名
2,6-Bornanedione
别名 Camphorquinone
6-Oxocamphor
CQ
CPQ
识别
CAS号 10373-78-1  
PubChem 25208
SMILES
性质
化学式 C10H14O2
摩尔质量 166.22 g·mol−1
熔点 196-198 °C(469-471 K)[1]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

参考文献

  1. ^ Jarugu Narasimha Moorthy, Nidhi Singhal, Kalyan Senapati. Oxidative cleavage of vicinal diols: IBX can do what Dess–Martin periodinane (DMP) can. Org. Biomol. Chem. 2007, 5 (5): 767–771 [2022-04-10]. ISSN 1477-0520. doi:10.1039/B618135J (英语). 
  2. ^ Jakubiak, J.; Allonas, X.; Fouassier, J.P.; Sionkowska, A.; Andrzejewska, E.; Linden, L.Å.; Rabek, J.F. Camphorquinone–amines photoinitating systems for the initiation of free radical polymerization. Polymer. August 2003, 44 (18): 5219–5226. doi:10.1016/S0032-3861(03)00568-8. 
  3. ^ Hongjin Chen, Wenyuan Wang, Jianjun Zhu, Yiying Han, Jian Liu. Electropolymerization of D-A type EDOT-based monomers consisting of camphor substituted quinoxaline unit for electrochromism with enhanced performance. Polymer. 2022-02, 240: 124485 [2022-04-10]. doi:10.1016/j.polymer.2021.124485 (英语). 
  4. ^ D. T. C. Yang, C. J. Zhang, P. P. Fu, G. W. Kabalka. Oxidation of α-Substituted Carbonyl Compounds to Carboxylic Acids in Aqueous Media Using Ultrasound. Synthetic Communications. 1997-05, 27 (9): 1601–1605 [2022-04-10]. ISSN 0039-7911. doi:10.1080/00397919708006098 (英语). 
  5. ^ Duggan, Andrew R.; Mciteka, Lulama P.; Lobb, Kevin A.; Kaye, Perry T. 1H NMR-based kinetic-mechanistic study of the intramolecular trans-esterification of 2-exo-3-exo-dihydroxybornane monoacrylate esters. South African Journal of Chemistry, 2013. 66: 140-144. ISSN 0379-4350.

樟脑醌, 是一种有机化合物, 化学式为c10h14o2, 它在牙科材料中用作光引发剂, 它可由樟脑在乙酸中经二氧化硒氧化制得, 它可以被次氯酸钠进一步氧化为樟脑酸, 它的两个羰基, 也能被氢化铝锂还原为羟基, iupac名2, bornanedione别名, camphorquinone6, oxocamphorcqcpq识别cas号, 10373, pubchem, 25208smiles, c2ccc1, c性质化学式, c10h14o2摩尔质量, 1熔点, 若非注明, 所有数据均出自标准状态, 参考文献, 编. 樟脑醌是一种有机化合物 化学式为C10H14O2 它在牙科材料中用作光引发剂 2 它可由樟脑在乙酸中经二氧化硒氧化制得 3 它可以被次氯酸钠进一步氧化为樟脑酸 4 它的两个羰基 C O 也能被氢化铝锂还原为羟基 C OH 5 樟脑醌IUPAC名2 6 Bornanedione别名 Camphorquinone6 OxocamphorCQCPQ识别CAS号 10373 78 1 PubChem 25208SMILES CC1 C2CCC1 C O C2 O C C性质化学式 C10H14O2摩尔质量 166 22 g mol 1熔点 196 198 C 469 471 K 1 若非注明 所有数据均出自标准状态 25 100 kPa 下 参考文献 编辑 Jarugu Narasimha Moorthy Nidhi Singhal Kalyan Senapati Oxidative cleavage of vicinal diols IBX can do what Dess Martin periodinane DMP can Org Biomol Chem 2007 5 5 767 771 2022 04 10 ISSN 1477 0520 doi 10 1039 B618135J 英语 Jakubiak J Allonas X Fouassier J P Sionkowska A Andrzejewska E Linden L A Rabek J F Camphorquinone amines photoinitating systems for the initiation of free radical polymerization Polymer August 2003 44 18 5219 5226 doi 10 1016 S0032 3861 03 00568 8 Hongjin Chen Wenyuan Wang Jianjun Zhu Yiying Han Jian Liu Electropolymerization of D A type EDOT based monomers consisting of camphor substituted quinoxaline unit for electrochromism with enhanced performance Polymer 2022 02 240 124485 2022 04 10 doi 10 1016 j polymer 2021 124485 英语 D T C Yang C J Zhang P P Fu G W Kabalka Oxidation of a Substituted Carbonyl Compounds to Carboxylic Acids in Aqueous Media Using Ultrasound Synthetic Communications 1997 05 27 9 1601 1605 2022 04 10 ISSN 0039 7911 doi 10 1080 00397919708006098 英语 Duggan Andrew R Mciteka Lulama P Lobb Kevin A Kaye Perry T 1H NMR based kinetic mechanistic study of the intramolecular trans esterification of 2 exo 3 exo dihydroxybornane monoacrylate esters South African Journal of Chemistry 2013 66 140 144 ISSN 0379 4350 取自 https zh wikipedia org w index php title 樟脑醌 amp oldid 75297414, 维基百科,wiki,书籍,书籍,图书馆,

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