4-氯苯甲醛
化合物
4-氯苯甲醛是一種有機化合物,化學式為C7H5ClO。它可由4-氯苯甲醇的氧化反應製得。[1][2]它可以進一步被氧化為4-氯苯甲酸。[3]它可以和丙二腈發生縮合反應,生成4-氯亞苯甲基丙二腈;[4]和苄胺反應,得到N-(4-氯亞苯甲基)苄胺。[5]
4-氯苯甲醛 | |
---|---|
識別 | |
CAS編號 | 104-88-1 |
性質 | |
化學式 | C7H5ClO |
莫耳質量 | 140.57 g·mol−1 |
熔點 | 47.5 °C(321 K) |
沸點 | 213.5 °C(487 K) |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
- ^ Y. X. Yang, X. Q. An, M. Kang, W. Zeng, Z. W. Yang, H. C. Ma. A Simple and Effective Method for Catalytic Oxidation of Alcohols Using the Oxone/Bu4NHSO4 Oxidation System. Russian Journal of Organic Chemistry. 2020-03, 56 (3): 521–523 [2021-05-10]. ISSN 1070-4280. doi:10.1134/S1070428020030240 (英語).
- ^ Juan V. Alegre-Requena, Eugenia Marqués-López, Raquel P. Herrera. Organocatalyzed Enantioselective Aldol and Henry Reactions Starting from Benzylic Alcohols. Advanced Synthesis & Catalysis. 2018-01-04, 360 (1): 124–129 [2021-05-10]. doi:10.1002/adsc.201701351 (英語).
- ^ Mahdi Hajimohammadi, Naeleh Azizi, Sajjad Tollabimazraeno, Ali Tuna, Jiri Duchoslav, Günther Knör. Cobalt (II) Phthalocyanine Sulfonate Supported on Reduced Graphene Oxide (RGO) as a Recyclable Photocatalyst for the Oxidation of Aldehydes to Carboxylic Acids. Catalysis Letters. 2021-01, 151 (1): 36–44 [2021-05-10]. ISSN 1011-372X. doi:10.1007/s10562-020-03287-9 (英語).
- ^ Ziyang Gao, Hongyuan Yang, Qing Liu. Natural Seashell Waste as an Efficient and Low‐Cost Catalyst for the Synthesis of Arylmethylenemalonitriles. CLEAN – Soil, Air, Water. 2019-10, 47 (10): 1900129 [2021-05-10]. ISSN 1863-0650. doi:10.1002/clen.201900129. (原始內容存檔於2022-03-28) (英語).
- ^ Meixia He, Jean-Marie Lehn. Time-Dependent Switching of Constitutional Dynamic Libraries and Networks from Kinetic to Thermodynamic Distributions. Journal of the American Chemical Society. 2019-11-20, 141 (46): 18560–18569 [2021-05-10]. ISSN 0002-7863. doi:10.1021/jacs.9b09395. (原始內容存檔於2022-03-28) (英語).