3-甲氧基氯化苄
外观
3-甲氧基氯化苄 | |
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识别 | |
CAS号 | 824-98-6 ![]() |
SMILES |
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性质 | |
化学式 | C8H9ClO |
摩尔质量 | 156.61 g·mol−1 |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
3-甲氧基氯化苄是一种有机氯化合物,化学式为C8H9ClO。它可由3-甲氧基苯甲醇和氯化亚砜在三乙胺的存在下于二氯甲烷中反应得到。[1]它和叠氮化钠在二甲基亚砜中反应,可以得到3-甲氧基苄基叠氮化物。[2]
参考文献
[编辑]- ^ Sylvain Picon; et al. Discovery, Structure-Activity Relationships, and In Vivo Activity of Dihydropyridone Agonists of the Bile Acid Receptor TGR5. Journal of Medicinal Chemistry (2023), 66 (17), 11732-11760. doi:10.1021/acs.jmedchem.2c01881.
- ^ Chao Niu, Gen Li, Adila Tuerxuntayi, Haji A. Aisa. Synthesis and Bioactivity of New Chalcone Derivatives as Potential Tyrosinase Activator Based on the Click Chemistry. Chinese Journal of Chemistry (2015), 33 (4), 486-494. doi:10.1002/cjoc.201400820.