2-Heptyl-2,3-dihydrobenzopyran-6-carboxylic acid | 158634-44-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 2-Heptyl-2,3-dihydrobenzopyran-6-carboxylic acid
• 英文别名: 2-heptyl-3,4-dihydro-2H-chromene-6-carboxylic acid
• CAS: 158634-44-7
• 化学式: C₁₇H₂₄O₃
• 分子量: 276.376
• InChiKey: NHMXCJOQHZZFPV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  20
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-Heptyl-2,3-dihydrobenzopyran-6-carboxylic acid 在 氯化亚砜 、 三乙胺 作用下， 以 乙腈 为溶剂， 反应 1.0h， 生成 2-Heptyl-2,3-dihydrobenzopyran-6-carboxylic acid 4'-(dodecyloxy)biphenyl-4-yl ester
  参考文献：
  名称：

  Synthesis and Properties of a New Family of Chiral Mesogens Containing the 2,3-Dihydrobenzopyran Nucleus

  摘要：

  A new class of mesogens A with a central chiral core based on the 2,3-dihydrobenzopyran nucleus was synthesized both in the racemic and optically pure form, and the thermotropic properties were studied. The distortion from structural linearity due to the presence of the 2,3-dihydropyran ring does not inhibit the existence of mesophases, and Ch, S-A, and S-C phases were observed according to the substituents present. The conformational constrictions imposed by cyclization proved not to be very important in determining the compactness of the cholesteric helix.

  DOI：

  10.1021/jo00099a022
• 作为产物：
  描述：

  2-heptyl-4H-chromen-4-one 在 palladium on activated charcoal 盐酸 、 正丁基锂 、 氢气 、 溴 作用下， 以 乙醚 、 乙醇 为溶剂， 25.0 ℃ 、200.0 kPa 条件下， 反应 60.75h， 生成 2-Heptyl-2,3-dihydrobenzopyran-6-carboxylic acid
  参考文献：
  名称：

  Synthesis and Properties of a New Family of Chiral Mesogens Containing the 2,3-Dihydrobenzopyran Nucleus

  摘要：

  A new class of mesogens A with a central chiral core based on the 2,3-dihydrobenzopyran nucleus was synthesized both in the racemic and optically pure form, and the thermotropic properties were studied. The distortion from structural linearity due to the presence of the 2,3-dihydropyran ring does not inhibit the existence of mesophases, and Ch, S-A, and S-C phases were observed according to the substituents present. The conformational constrictions imposed by cyclization proved not to be very important in determining the compactness of the cholesteric helix.

  DOI：

  10.1021/jo00099a022

文献信息

• Bonini Bianca F., Carboni Paolo, Gottarelli Giovanni, Masiero Stefano, Sp+, J. Org. Chem, 59 (1994) N 20, S 5930-5936
  作者：Bonini Bianca F., Carboni Paolo, Gottarelli Giovanni, Masiero Stefano, Sp+

  DOI：——

  日期：——
• Synthesis and Properties of a New Family of Chiral Mesogens Containing the 2,3-Dihydrobenzopyran Nucleus
  作者：Bianca F. Bonini、Paolo Carboni、Giovanni Gottarelli、Stefano Masiero、Gian Piero Spada

  DOI：10.1021/jo00099a022

  日期：1994.10

  A new class of mesogens A with a central chiral core based on the 2,3-dihydrobenzopyran nucleus was synthesized both in the racemic and optically pure form, and the thermotropic properties were studied. The distortion from structural linearity due to the presence of the 2,3-dihydropyran ring does not inhibit the existence of mesophases, and Ch, S-A, and S-C phases were observed according to the substituents present. The conformational constrictions imposed by cyclization proved not to be very important in determining the compactness of the cholesteric helix.