1-(3,5-dimethoxyphenyl)-1-heptanol | 129478-11-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-(3,5-dimethoxyphenyl)-1-heptanol
• 英文别名: 1-(3,5-dimethoxyphenyl)heptan-1-ol
• CAS: 129478-11-1
• 化学式: C₁₅H₂₄O₃
• mdl: MFCD21484137
• 分子量: 252.354
• InChiKey: BOCWWFRBCODDRQ-UHFFFAOYSA-N

物化性质

• 沸点：
  372.4±37.0 °C(Predicted)
• 密度：
  1.005±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  18
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(3,5-dimethoxyphenyl)-1-heptanol 在 chromium(VI) oxide 、 硫酸 作用下， 以 丙酮 为溶剂， 反应 0.5h， 以79.6%的产率得到1-(3,5-二甲氧基苯基)庚烷-1-酮
  参考文献：
  名称：

  Pharmacophoric Requirements for Cannabinoid Side Chains:  Multiple Bond and C1‘-Substituted Δ⁸-Tetrahydrocannabinols

  摘要：

  Accumulated evidence indicates that within the cannabinoid structure the aliphatic side chain plays a pivotal role in determining cannabimimetic activity. We describe the synthesis and affinities for the CB1 and CB2 receptors of a series of novel Delta(8)-THC analogues in which the side-chain pharmacophores are conformationally more defined than in the parent molecule. No analogue has the side-chain pharmacophore in a fully restricted conformation. However, our design serves to narrow down the scope of options for conformational requirements at the receptor active sites. All the analogues tested showed nanomolar or subnanomolar affinities for the receptors; 2-(6a,7,10,10a-tetrahydro-6,6,9-trimethyl-1-hydroxy-6H-dibenzo[b,d]pyranyl)- 2-hexyl-1,3-dithiolane was found to possess very high affinity for both cannabinoid receptors(CB1, K-i = 0.32 nM; CB2, K-i = 0.52 nM).

  DOI：

  10.1021/jm970277i
• 作为产物：
  描述：

  3,5-二甲氧基苯甲酰氯 在 氢氧化钾 作用下， 以 四氢呋喃 为溶剂， 反应 2.0h， 生成 1-(3,5-dimethoxyphenyl)-1-heptanol
  参考文献：
  名称：

  A cytotoxic constituent of Lysimachia japonica Thunb. (Primulaceae) and the structure-activity relationships of related compounds.

  摘要：

  从 Lysimachia japonica THUNB.（报春花科）中分离出一种具有细胞毒性的烷基间苯二酚，并确定其为 grevillol (2)。(体外测试了它对 KB、B-16、PC-13、L-5178Y、P-388 和 HEp-2 细胞的细胞毒性。还测试了合成的相关化合物对 KB 细胞系的细胞毒性，并讨论了其结构-活性关系。

  DOI：

  10.1248/cpb.37.2431

文献信息

• Synthesis and pharmacology of the isomeric methylheptyl-Δ8-tetrahydrocannabinols
  作者：John W. Huffman、John Liddle、Sammy G. Duncan、Shu Yu、Billy R. Martin、Jenny L. Wiley

  DOI：10.1016/s0968-0896(98)80014-x

  日期：1998.12

  The synthesis of the 3-heptyl, and the eleven isomeric 3-methylheptyl-delta8-tetrahydrocannabinols (3-7, R and S methyl epimers, and 8) has been carried out. The synthetic approach entailed the synthesis of substituted resorcinols, which were subjected to acid catalyzed condensation with trans-para-menthadienol to provide the delta8-THC analogue. The 1'-, 2'- and 3'-methylheptyl analogues (3-5) are

  已经进行了3-庚基和十一种异构的3-甲基庚基-δ8-四氢大麻酚（3-7，R和S甲基差向异构体和8）的合成。合成方法需要合成间苯二酚，将其与反式对-薄荷脑进行酸催化的缩合反应，以提供δ8-THC类似物。1'-，2'-和3'-甲基庚基类似物（3-5）比delta8-THC更有效。4′-，5′-和6′-甲基庚基异构体（6-8）的效力与δ8-THC近似相等。
• 5-Alkylresorcinols from Hakea trifurcata, that cleave DNA.
  作者：William Lytollis、Ralph T. Scannell、Haoyun An、V. S. Murty、K. Sambi Reddy、John R. Barr、Sidney M. Hecht

  DOI：10.1021/ja00156a004

  日期：1995.12

  A dichloromethane extract of Hakea trifurcata that mediated relaxation of phi X174 replicative form DNA at micromolar concentrations in the presence of CU2+ was resolved into six active components by bioassay-guided fractionation. Five of the active principles were characterized structurally and shown to be 5-alkylresorcinol derivatives. These included 1,3-dihydroxy-5-tridecylbenzene (1), 1,3-dihydroxy-5-(cis-8'-pentadecenyl)benzene (2), 1,3-dihydroxy-5-[14'-(3'',5''-dihydroxyphenyl)-cis-6'-tetradecenyl]benzene (3), 1,3-dihyroxy-5-[1 4'-(3'',5''-dihydroxyphenyl)tetradecyl]benzene (4), and 1,3-dihydroxy-5-[16'-(3'',5''-dihydroxyphenyl)-cis-8'-hexadencenyl]benzene (5). The structures of these five natural principles were confirmed by total synthesis; compounds 1-5 were accessible from 3,5-dimethoxybenzaldehyde in overall yields of 59%, 27%, 15%, 16%, and 13%, respectively.
• ARISAWA, MUNEHISA;OHMURA, KAZUNOBU;KOBAYASHI, AKIO;MORITA, NAOKATA, CHEM. AND PHARM. BULL., 37,(1989) N, C. 2431-2434
  作者：ARISAWA, MUNEHISA、OHMURA, KAZUNOBU、KOBAYASHI, AKIO、MORITA, NAOKATA

  DOI：——

  日期：——