1-heptadecyl methanesulfonate | 62732-71-2

• 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: 1-heptadecyl methanesulfonate
• 英文别名: Heptadecyl methanesulfonate；heptadecyl methanesulfonate
• CAS: 62732-71-2
• 化学式: C₁₈H₃₈O₃S
• 分子量: 334.564
• InChiKey: CLQHOYBUBUGWNS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.9
• 重原子数：
  22
• 可旋转键数：
  17
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  51.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-heptadecyl methanesulfonate 、 (6-deoxy-α-D-gluco-heptopyranosyluronic acid)-6-deoxy-α-D-gluco-heptopyranosiduronic acid 在 potassium carbonate 作用下， 生成 1-heptadecyl <(1-heptadecyl 6-deoxy-α-D-gluco-heptopyranosyluronate)-6-deoxy-α-D-gluco-heptopyranosid>uronate
  参考文献：
  名称：

  Synthesis of alkyl [(alkyl 6-deoxy-α-d-gluco-heptopyranosyl-uronate) 6-deoxy-α-d-gluco-heptopyranosid]uronates, a novel type of mirror pseudo cord factor

  摘要：

  The 1-octyl, 1-pentadecyl, 1-hexadecyl, 1-heptadecyl, and 1-octadecyl diesters of (6-deoxy-alpha-D-gluco-heptopyranosyluronic acid) 6-deoxy-alpha-D-gluco-heptopyranosiduronic acid, a new homolog of trehalosuronic acid, were prepared by two procedures. One procedure involved conversion of the peracetylated acid into its dichloride, reaction of the latter with the alkanols, and acid-catalyzed deacetylation of the products, whereas the other consisted of reaction of alkyl mesylates with the potassium salt of the unprotected acid.

  DOI：

  10.1016/0008-6215(91)80155-g
• 作为产物：
  描述：

  1-十七烷醇 、 甲基磺酰氯 以 吡啶 为溶剂， 反应 1.0h， 生成 1-heptadecyl methanesulfonate
  参考文献：
  名称：

  Synthesis of alkyl [(alkyl 6-deoxy-α-d-gluco-heptopyranosyl-uronate) 6-deoxy-α-d-gluco-heptopyranosid]uronates, a novel type of mirror pseudo cord factor

  摘要：

  The 1-octyl, 1-pentadecyl, 1-hexadecyl, 1-heptadecyl, and 1-octadecyl diesters of (6-deoxy-alpha-D-gluco-heptopyranosyluronic acid) 6-deoxy-alpha-D-gluco-heptopyranosiduronic acid, a new homolog of trehalosuronic acid, were prepared by two procedures. One procedure involved conversion of the peracetylated acid into its dichloride, reaction of the latter with the alkanols, and acid-catalyzed deacetylation of the products, whereas the other consisted of reaction of alkyl mesylates with the potassium salt of the unprotected acid.

  DOI：

  10.1016/0008-6215(91)80155-g

文献信息

• BAER, HANS H.;BRETON, ROGER L., CARBOHYDR. RES., 209,(1991) C. 181-189
  作者：BAER, HANS H.、BRETON, ROGER L.

  DOI：——

  日期：——
• Synthesis of alkyl [(alkyl 6-deoxy-α-d-gluco-heptopyranosyl-uronate) 6-deoxy-α-d-gluco-heptopyranosid]uronates, a novel type of mirror pseudo cord factor
  作者：Hans H. Baer、Roger L. Breton

  DOI：10.1016/0008-6215(91)80155-g

  日期：1991.1

  The 1-octyl, 1-pentadecyl, 1-hexadecyl, 1-heptadecyl, and 1-octadecyl diesters of (6-deoxy-alpha-D-gluco-heptopyranosyluronic acid) 6-deoxy-alpha-D-gluco-heptopyranosiduronic acid, a new homolog of trehalosuronic acid, were prepared by two procedures. One procedure involved conversion of the peracetylated acid into its dichloride, reaction of the latter with the alkanols, and acid-catalyzed deacetylation of the products, whereas the other consisted of reaction of alkyl mesylates with the potassium salt of the unprotected acid.