異丁酸鈉
化合物
異丁酸鈉是一種羧酸鹽,化學式為C4H7NaO2。它可由異丁酸和氫氧化鈉反應製得。[1]它和硝酸鐵或高氯酸鐵反應,可以得到[Fe3O(C4H7O2)6(H2O)3]A(A=ClO4, NO3)。[2]它和硼烷的四氫呋喃溶液反應,可以得到異丁酸硼氫化鈉,它經PCC氧化可以得到異丁醛。[3]
異丁酸鈉 | |
---|---|
別名 | 2-甲基丙酸鈉 |
識別 | |
CAS號 | 996-30-5 |
性質 | |
化學式 | C4H7NaO2 |
摩爾質量 | 110.09 g·mol−1 |
外觀 | 粉末[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
- ^ 1.0 1.1 Chad E. Davis, Bryan C. Duffy, Robert M. Coates. Total Synthesis of (±)-Cameroonan-7α-ol and Biomimetic Rearrangements to Related Nopsane Sesquiterpenes. The Journal of Organic Chemistry. 2003-09-01, 68 (18): 6935–6943 [2023-02-27]. ISSN 0022-3263. doi:10.1021/jo0343580. (原始內容存檔於2023-02-26) (英語).
- ^ Anastasia N. Georgopoulou, Yiannis Sanakis, Vassilis Psycharis, Catherine P. Raptopoulou, Athanassios K. Boudalis. Mössbauer spectra of two extended series of basic iron(III) carboxylates [Fe3O(O2CR)6(H2O)6]A (A− = ClO4 −, NO3 −). Hyperfine Interactions. 2010-06, 198 (1-3): 229–241 [2023-02-27]. ISSN 0304-3843. doi:10.1007/s10751-010-0179-2 (英語).
- ^ Cha J S, Park J H, Mun S J. Transformation of carboxylic acid salts to aldehydes by stepwise reduction with borane and oxidation with pyridinium chlorochromate. Bulletin of the Korean Chemical Society, 2001, 22(10): 1089-1092.
拓展閱讀
- Vorlander, D. Behavior of Salts of Organic Acids when Melted. Berichte der Deutschen Chemischen Gesellschaft. 1911, 43: 3120–3135. ISSN 0365-9496..
- George A. Blondin, William J. Vail, David E. Green. The mechanism of mitochondrial swelling. Archives of Biochemistry and Biophysics. 1969-01, 129 (1): 158–172 [2023-02-27]. doi:10.1016/0003-9861(69)90162-3. (原始內容存檔於2018-07-01) (英語).