n-Butylsulfonatanion | 24613-77-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机磺酸及其衍生物
• 英文名称: n-Butylsulfonatanion
• 英文别名: butane-1-sulfonate(1-)；butane-1-sulfonic acid anion；Butane-1-sulfonate
• CAS: 24613-77-2
• 化学式: C₄H₉O₃S
• 分子量: 137.18
• InChiKey: QDHFHIQKOVNCNC-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  8
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  65.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  nickel(II) chloride hexahydrate 、 cobalt(II) chloride hexahydrate 、 n-Butylsulfonatanion 在 乌洛托品 、 溴 作用下， 以 水 、 乙腈 、 乙醇 为溶剂， 反应 53.0h， 生成
  参考文献：
  名称：

  通过增加基础间距来提高钴镍层状双氢氧化物的矫顽力†

  摘要：

  与表现出依赖于结构的磁性的层状金属氢氧化物盐相比，包含过渡金属离子的层状双氢氧化物（LDH）的磁性仍然可以发展。在本文中，我们报告了由Co-Ni LDH和正烷基磺酸根阴离子（Co-Ni-C n SO 3 LDH）组成的混合磁体的制备。由于Co-Ni LDH是阴离子可交换的，因此我们可以通过嵌入n来系统地控制层间距-具有不同碳数的-烷基磺酸盐。用与温度和场有关的磁化强度测量来检验磁性能。结果，我们发现矫顽场取决于基础间距。建议增加基础间距会改变平面内超交换相互作用与远程平面外偶极相互作用之间的竞争。此外，矫顽场在基距20Å附近的跃迁被认为是Co-Ni-C n SO 3 LDH中磁有序的修正。

  DOI：

  10.1039/c6dt01723a
• 作为产物：
  描述：

  正溴丁烷 、 ammonium sulfite 以86.5%的产率得到n-Butylsulfonatanion
  参考文献：
  名称：

  SULFUR STUDIES. XV. THE SYNTHESIS OF ALKANE-SULFONIC ACIDS AND CERTAIN DERIVATIVES^*

  摘要：

  DOI：

  10.1021/jo01207a003

文献信息

• MOLECULAR CONTAINERS AND METHODS OF MAKING AND USING SAME
  申请人：Isaacs Lyle David

  公开号：US20140094529A1

  公开（公告）日：2014-04-03

  Acyclic CB[n]-type compounds, methods of making such compounds, and uses of the compounds. For example, these compounds can be used as nanocontainers to solubilize pharmaceutical agents. Also provided are compositions and methods of using them for therapy or prophylaxis of a wide variety of conditions for which therapy or prophylaxis is desirable.

  无环CB[n]型化合物，制备这种化合物的方法以及这种化合物的用途。例如，这些化合物可以用作纳米容器，溶解药物。还提供了组成物和使用它们治疗或预防各种需要治疗或预防的疾病的方法。
• Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: S: MVol.B2, 3.1.3, page 603 - 607
  作者：

  DOI：——

  日期：——
• THE STABILITY OF THE CARBON--SULFUR BOND IN SOME ALIPHATIC SULFONIC ACIDS
  作者：F. C. Wagner、E. Emmet. Reid

  DOI：10.1021/ja01360a026

  日期：1931.9
• Micellar effects on the reaction of (arylsulfonyl)alkyl arenesulfonates with hydroxide ion. 2. The absence of substrate orientational effects in a series of sulfonates of different hydrophobicities
  作者：Frank M. Witte、Jan B. F. N. Engberts

  DOI：10.1021/jo00221a032

  日期：1985.10
• Characterization of a Two-component Alkanesulfonate Monooxygenase from Escherichia coli
  作者：Eric Eichhorn、Jan R. van der Ploeg、Thomas Leisinger

  DOI：10.1074/jbc.274.38.26639

  日期：1999.9

  The Escherichia coli ssuEADCB gene cluster is required for the utilization of alkanesulfonates as sulfur sources, and is expressed under conditions of sulfate or cysteine starvation. The SsuD and SsuE proteins were overexpressed and characterized. SsuE was purified to homogeneity as an N-terminal histidine-tagged fusion protein. Native SsuE was a homodimeric enzyme of ill, 58,400, which catalyzed an NAD(P)H-dependent reduction of FMN, but it was also able to reduce FAD or riboflavin, The SsuD protein was purified to >98% purity using cation exchange, anion exchange, and hydrophobic interaction chromatography. The pure enzyme catalyzed the conversion of pentanesulfonic acid to sulfite and pentaldehyde and was able to desulfonate a wide range of sulfonated substrates including C-2 to C-10 unsubstituted linear alkanesulfonates, substituted ethanesulfonic acids and sulfonated buffers. SsuD catalysis was absolutely dependent on FMNH2 and oxygen, and was maximal for SsuE/SsuD molar ratios of 2.1 to 4.2 in 10 mM Tris-HCl, pH 9.1. Native SsuD was a homotetrameric enzyme of M-r 181,000. These results demonstrate that SsuD is a broad range FMNH2-dependent monooxygenase catalyzing the oxygenolytic conversion of alkanesulfonates to sulfite and the corresponding aldehydes, SsuE is the FMN reducing enzyme providing SsuD with FMNH2.