3-甲硫基丙醇
3-甲硫基丙醇 | |
---|---|
IUPAC名 3-methylsulfanylpropan-1-ol | |
識別 | |
CAS號 | 505-10-2 |
PubChem | 10448 |
ChemSpider | 10016 |
SMILES |
|
Beilstein | 1731208 |
ChEBI | 49019 |
性質 | |
化學式 | C4H10OS |
摩爾質量 | 106.19 g·mol−1 |
危險性 | |
GHS危險性符號 | |
GHS提示詞 | 警告 |
H-術語 | H315, H319, H335 |
相關物質 | |
相關化學品 | 1-(Methylthio)propane; Methional; Methionine; 1,3-Propanediol mono methyl ether; 4-(Methylsulfanyl)butanoic acid; 4-Thiapentanoic acid; |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
3-甲硫基丙醇是一種有機化合物,化學式為C4H10OS。它可由3-甲硫基丙醛的還原反應製得,[1]或以3-氯丙醇和甲硫醇鈉為原料反應得到。[2]它可以被N-氟代二苯磺酰胺(NFSI)氧化為甲基羥丙基碸。[3]
參考文獻
- ^ Brandts, J. A. M.; Cavenaghi, C. V.; Gerlach, A.; Burk, M. J. Tethering technology: Anchored chiral and achiral homogeneous catalysts applied in enantio- and chemoselective hydrogenation reactions. Chimica Oggi, 2000. 18 (10): 47-49. ISSN 0392-839X.
- ^ Herbert C. Brown, Gary J. Lynch. Solvomercuration-demercuration. 9. Oxymercuration-demercuration of chloro-, epoxy-, and thiomethyl-substituted alkenes. The Journal of Organic Chemistry. 1981-02, 46 (5): 930–939 [2022-03-29]. ISSN 0022-3263. doi:10.1021/jo00318a019. (原始內容存檔於2022-03-29) (英語).
- ^ Xiaobo Xu, Leyu Yan, Shengqiang Wang, Panpan Wang, A-Xiu Yang, Xiaolong Li, Hao Lu, Zhong-Yan Cao. Selective synthesis of sulfoxides and sulfones via controllable oxidation of sulfides with N -fluorobenzenesulfonimide. Organic & Biomolecular Chemistry. 2021, 19 (40): 8691–8695 [2022-03-29]. ISSN 1477-0520. doi:10.1039/D1OB01632F (英語).