1-bromo-2-(methanesulfonylsulfanyl)ethane

• ChemBase编号: 162876
• 分子式: C3H7BrO2S2
• 平均质量: 219.12048
• 单一同位素质量: 217.90708346
• SMILES: CS(=O)(=O)SCCBr
• Canonical SMILES: BrCCSS(=O)(=O)C
• InChI: InChI=1S/C3H7BrO2S2/c1-8(5,6)7-3-2-4/h2-3H2,1H3
• InChIKey: YMXDGRXCNRNUFC-UHFFFAOYSA-N

名称和登记号

名称

• IUPAC标准名: 1-bromo-2-(methanesulfonylsulfanyl)ethane
• IUPAC传统名: 1-bromo-2-(methanesulfonylsulfanyl)ethane
• 别名: Methanesulfonothioic Acid S-(2-Bromoethyl) Ester; 2-Bromoethyl Methanethiosulfonate

登记号

• CAS号: 26139-15-1
• PubChem SID: 162257011
• PubChem CID: 4114054

理论计算性质

• 质子受体: 2
• 质子供体: 0
• LogD (pH = 5.5): 0.53381485
• LogD (pH = 7.4): 0.53381485
• Log P: 0.53381485
• 摩尔折射率: 39.9499 cm^3
• 极化性: 16.537893 Å^3
• 极化表面积: 34.14 Å^2
• 可自由旋转的化学键: 3
• 里宾斯基五规则: true

分子性质

理化性质

• 溶解度: Ethyl Acetate; Methanol
• 外观: Pale Brown Oily Solid

详细说明

Toronto Research Chemicals - B684250

Reacts specifically and rapidly with thiols to form mixed disulfides. Used to probe the structures of the ACh receptor channel of the GABA receptor channel and of lactose permease. Useful for mapping the pore-lining regions of the ryanodine receptor.

参考文献

• Yang, N. et al.: Neuron, 16, 113 (1996)
• Kuner, T. et al.: Neuron, 17, 343 (1996)
• Holmgren, M. et al: Neuropharmacology, 35, 797 (1996) Chahine, M. et al.: Biochemical & Biophysical Res. Commun., 233, 606 (1996)
• Ehrlich, B.E., et al.: J. Gen. Physiol.,