cis-3,4-dimethylthiolane | 5161-11-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 硫杂环戊烷
• 英文名称: cis-3,4-dimethylthiolane
• 英文别名: cis-β,β'-Dimethylthiophan；cis-3,4-Dimethyl-thiacyclopentane；(3R,4S)-3,4-dimethylthiolane
• CAS: 5161-11-5
• 化学式: C₆H₁₂S
• 分子量: 116.227
• InChiKey: UCTWEFUUQKCEGE-OLQVQODUSA-N

物化性质

• 熔点：
  -82.87°C (estimate)
• 沸点：
  167.34°C (estimate)
• 密度：
  0.9142
• 保留指数：
  950

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  7
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  25.3
• 氢给体数：
  0
• 氢受体数：
  1

安全信息

• 海关编码：
  2934999090

反应信息

• 作为反应物：
  描述：

  cis-3,4-dimethylthiolane 、 碘甲烷 以 乙醇 为溶剂， 生成 1,cis-3,cis-4-trimethylthiolanium iodide 、 1,trans-3,trans-4-trimethylthiolanium iodide
  参考文献：
  名称：

  13C chemical shifts and conformational analysis ofS-methylthiolanium cations

  摘要：

  AbstractThe 13C NMR spectra of all cations obtained by methylation at sulphur of the mono‐and dimethylthiolanes are reported. The methyl substituent on sulphur affects the shieldings of the adjacent carbons in a manner which allows easy identification of the cis and trans isomers. For most compounds the 13C pattern is consistent with a half‐chair ring conformation with maximum staggering at C‐3, C‐4. Only with methyl groups at the 1,2‐or 1,2,3‐positions is the half‐chair appreciably deformed. It is suggested that in these cases the preferred conformation is a quasi‐envelope with C‐3 at the top.

  DOI：

  10.1002/mrc.1270150115
• 作为产物：
  描述：

  2,3-二甲基-1,4-丁二醇 在 sodium sulfide 作用下， 以 吡啶 为溶剂， 生成 cis-3,4-dimethylthiolane
  参考文献：
  名称：

  13C chemical shifts and conformational analysis of methyl substituted thiacyclopentanes

  摘要：

  AbstractThe 13C NMR spectra of thiacyclopentane (thiolane) and its mono‐ and dimethyl derivatives at positions other than the heteroatom are reported. The 13C shieldings are found to be consistent with a description of these compounds in terms of equilibria between half‐chair conformers. An attempt has been made to establish the axial or equatorial preference of methyl groups adjacent to, or removed from, the sulphur atom in these systems. In agreement with previous observations on thiacyclohexanes (thianes), the conformational preference of a methyl group for the equatorial orientation is greater at the β than at the α position.

  DOI：

  10.1002/mrc.1270130414

文献信息

• [EN] CLASS OF FUSED RING TRIAZOLE COMPOUND, PREPARATION METHOD, AND USE<br/>[FR] CLASSE DE COMPOSÉ DE TRIAZOLE CYCLIQUE FUSIONNÉ, PROCÉDÉ DE PRÉPARATION ET UTILISATION<br/>[ZH] 一类稠环三氮唑类化合物、制备方法和用途
  申请人：RUDONG RINGENE PHARMACEUTICALS CO LTD

  公开号：WO2020038458A1

  公开（公告）日：2020-02-27

  本发明公开了一类稠环三氮唑类化合物、制备方法和用途。本发明具体公开了一种如式(I)所示稠环三氮唑类化合物、或其药学上可接受的盐、或其对映异构体、非对映异构体、互变异构体、溶剂化物、多晶型物或前药、其制备方法及其在药学上的应用。(I)