3,4-二氟苯胺
（重新導向自C6H5F2N）
| 3,4-二氟苯胺 | |
|---|---|
| |
| 識別 | |
| CAS號 | 3863-11-4 
|
| 性質 | |
| 化學式 | C6H5F2N |
| 摩爾質量 | 129.11 g·mol−1 |
| 沸點 | 77 °C（7 mmHg）[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
3,4-二氟苯胺是一種有機氟化合物，化學式為C6H5F2N，它可由3,4-二氟硝基苯還原製得。[2][1]它和亞硝酸叔丁酯、三甲基疊氮矽烷在乙腈中反應，可以得到4-疊氮基-1,2-二氟苯。[3]
參考文獻
[編輯]- ^ 1.0 1.1 Arthur F. Helin; Calvin A. VanderWerf. Synthesis of 3,4-Difluorophenylarsonic Acid. J. Am. Chem. Soc. 1951, 73, 12, 5884–5885. doi:10.1021/ja01156a526.
- ^ Venepally, Vijayendar; Sirisha, K.; Kumar, C. Ganesh; Jala, Ram Chandra Reddy. Synthesis and antimicrobial evaluation of novel alkylated piperazine-based fluoroquinolone carboxylate derivatives. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 2020. 59B (4): 474-484. ISSN 0975-0983. CODEN IJSBDB.
- ^ Fan, Dongguang; et al. Structural and Activity Relationships of 6-Sulfonyl-8-Nitrobenzothiazinones as Antitubercular Agents. Journal of Medicinal Chemistry, 2021. 64 (19). doi:10.1021/acs.jmedchem.1c01049.