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S-亞硝基甲硫醇

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S-亞硝基甲硫醇
別名 硫代亞硝酸甲酯
識別
CAS號 22223-61-6  checkY
SMILES
 
  • CSN=O
性質
化學式 CH3NOS
摩爾質量 77.11 g·mol−1
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

S-亞硝基甲硫醇是一種有機化合物,化學式為CH3SNO,它是最簡單的S-亞硝基硫醇英語S-Nitrosothiol。它可由甲硫醇亞硝酸叔丁酯三氧化二氮反應[1][2]或苯基硫代亞磺酸甲酯和四氧化二氮反應[3]製得。它和二氧化氮反應,生成二甲基二硫一氧化氮[4]它和羰基(八乙基卟啉)合鋨反應,可以得到亞硝基(甲硫基)(八乙基卟啉)合鋨。[1]

參考文獻

  1. ^ 1.0 1.1 Jonghyuk Lee, Geun-Bae Yi, Douglas R Powell, Masood A Khan, George B Richter-Addo. Synthesis, characterization, and protonation of octaethylporphyrin osmium nitrosyl complexes containing axial thiolate ligands - X-ray structures of an alkyl thionitrite (RSNO) and its (OEP)Os(NO)(SR) addition product. Canadian Journal of Chemistry. 2001-05-01, 79 (5-6): 830–840 [2021-12-13]. ISSN 0008-4042. doi:10.1139/v00-168 (英語). 
  2. ^ R.J. Philippe. The infrared spectrum of methyl thionitrite. Journal of Molecular Spectroscopy. 1961-01, 6: 492–496 [2021-12-13]. doi:10.1016/0022-2852(61)90272-7. (原始內容存檔於2018-06-22) (英語). 
  3. ^ Shigeru Oae, Daikichi Fukushima, Yong H. Kim. MULTISTEP OXIDATIONS OF THE UNSYMMETRICAL DISULFIDE AND THIOLSULFINATES: NEW EVIDENCE FOR THE FORMATION OF THE THIONITRITE AND THE SULFINYL DERIVATIVES AS THE INTERMEDIATES. Chemistry Letters. 1978-03-05, 7 (3): 279–280 [2021-12-13]. ISSN 0366-7022. doi:10.1246/cl.1978.279 (英語). 
  4. ^ Balla, R. Jeffrey; Heicklen, Julian. Oxidation of sulfur compounds. 2. Thermal reactions of nitrogen dioxide with aliphatic sulfur compounds. The Journal of Physical Chemistry (American Chemical Society (ACS)). 1984, 88 (25): 6314–6317. ISSN 0022-3654. doi:10.1021/j150669a052. 

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