组氨酸钠
| 组氨酸钠 | |
|---|---|
| 识别 | |
| CAS号 | 1595072-69-7  23768-86-7（L）
|
| SMILES |
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| 性质 | |
| 化学式 | C6H8N3NaO2 |
| 摩尔质量 | 177.14 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
组氨酸钠是一种氨基酸盐，化学式为C6H8N3O2Na。
制备
它和二溴三(4-甲苯基)锑反应，可以得到二(组氨酸)三(4-甲苯基)锑[2]。它和醛反应，可以得到相应的席夫碱[3]。
参考文献
- ^ Balaev, A. N.; Okhmanovich, K. A.; Fedorov, V. E. Convenient Four-Step Synthesis of H-Pyr-His-Trp-OH, a Key Tripeptide Intermediate for the Production of Synthetic Gonadoliberin Agonists. Pharmaceutical Chemistry Journal. 2016-06, 50 (3): 192–194. doi:10.1007/s11094-016-1421-2.
- ^ Mushtaq, Rabia; Rauf, Muhammad Khawar; Bond, Marcus; Badshah, Amin; Ali, Muhammad Irshad; Nadhman, Akhtar; Yasinzai, Masoom; Tahir, Muhammad Nawaz. A structural investigation of heteroleptic pentavalent antimonials and their leishmanicidal activity: Synthesis of leishmanicidal heteroleptic pentavalent antimonials. Applied Organometallic Chemistry. 2016-06, 30 (6): 465–472. doi:10.1002/aoc.3456.
- ^ Borisova, Nataliya E.; Gulevich, Tatiana G.; Reshetova, Marina D.; Knizhnikov, Valeri A. Simple and Reliable Protocol for Metal-Free Assembling of the Bibrachial Schiff Bases and Their Reduced Derivatives Bearing Amino Acids or Short Peptide Residues. Synthetic Communications. 2013-01, 43 (3): 345–360. doi:10.1080/00397911.2011.597534.