(p-methoxybenzyloxy)-2-hydroxybutanol | 167629-46-1

• 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: (p-methoxybenzyloxy)-2-hydroxybutanol
• 英文别名: 4-(p-Methoxybenzyloxy)-1,2-butandiol；4-[(4-methoxyphenyl)methoxy]butane-1,2-diol
• CAS: 167629-46-1
• 化学式: C₁₂H₁₈O₄
• 分子量: 226.273
• InChiKey: YRHIJTKHDXQBLC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.6
• 重原子数：
  16
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  58.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (p-methoxybenzyloxy)-2-hydroxybutanol 在 吡啶 、 咪唑 、 戴斯-马丁氧化剂 作用下， 以 二氯甲烷 为溶剂， 生成 1-(tert-butyldiphenylsilyloxy)-4-(4-methoxy-benzyloxy)-butan-2-one
  参考文献：
  名称：

  Synthesis of aglycon analogues of sarmentosin and Their bioactivity of lymphocyte proliferation

  摘要：

  A number of aglycon analogues of sarmentosin were prepared and their bioactivities on the proliferation of T-lymphocytes and B-lymphocytes were assayed. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00801-6
• 作为产物：
  描述：

  1-(4-methoxybenzyloxy)-3-butene 在 四氧化锇 、 N-甲基吲哚酮 作用下， 以 水 、 丙酮 为溶剂， 以70%的产率得到(p-methoxybenzyloxy)-2-hydroxybutanol
  参考文献：
  名称：

  印度海草突触藻的新型β-咔啉胍衍生物tiruchanduramine的分离与合成

  摘要：

  一种新颖β咔啉胍生物碱，tiruchanduramine，从印度海鞘的有效α葡萄糖苷酶抑制剂，外消旋形式的分离和合成Synoicum长喙天蛾属已经实现。

  DOI：

  10.1016/j.tetlet.2005.06.060

文献信息

• An Efficient and Selective Method for Hydrolysis of Acetonides
  作者：Xiangshu Xiao、Donglu Bai

  DOI：10.1055/s-2001-12340

  日期：——

  Acetonide was selectively and efficiently cleaved with cerium (III) chloride heptahydrate and oxalic acid in acetonitrile. This method was found to be of good functionalities compatibility with such acid sensitive groups as Tr, PMB, TBDMS, TBDPS, OAc, OBz, OTs, OTf.

  丙酮酸二苯酯在乙腈中与七水合氯化铈（III）和草酸选择性且高效地进行裂解。发现这种方法与对酸敏感的基团如三苯甲基、对甲氧基苄基、叔丁基二甲基硅基、叔丁基二苯基硅基、乙酸酯、苯甲酸酯、对甲苯磺酸酯、三氟甲磺酸酯等具有良好的功能性兼容性。
• BENZENE DERIVATIVE
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：US20210332009A1

  公开（公告）日：2021-10-28

  A compound represented by general formula (I) (in the formula, all symbols are as described in the description) or a salt thereof has a potent nerve-protecting and/or -repairing activity, and therefore can be used as a therapeutic agent for neuropathy (e.g., chronic inflammatory demyelinating polyneuropathy, Guillain-Barre syndrome, periarteritis nodosa, allergic vasculitis, diabetic peripheral neuropathy, entrapment neuropathy, peripheral neuropathy associated with the administration of a chemotherapeutic drug, or peripheral neuropathy associated with Charcot-Marie-Tooth disease).

  通式（I）表示的化合物（在公式中，所有符号如描述中所述）或其盐具有强大的神经保护和/或修复活性，因此可用作神经病变的治疗剂（例如，慢性炎症性脱髓鞘性多发性神经病、吉兰-巴雷综合征、周围动脉炎、过敏性血管炎、糖尿病周围神经病变、神经卡压病变、与化疗药物治疗相关的周围神经病变，或与沙科-玛丽-图斯病相关的周围神经病变）。
• Carbo-acyclic nucleoside derivatives as antiviral and antineoplastic
  申请人：Hoechst Marion Roussel, Inc.

  公开号：US06017923A1

  公开（公告）日：2000-01-25

  ##STR1## The present invention is directed to a class of novel carbocyclic derivatives having formulas (I) and (II) and their use as anti-viral and anti-neoplastic agents, wherein X.sub.1 and X.sub.2 are each independently hydrogen, fluorine, or chlorine, R is hydrogen or hydroxymethyl, J is a radical of formulas (a), (b) and (c). Y.sub.1 is a CH group, a CCl group, a CBr group or a CNH.sub.2 group, Y.sub.2 and Y.sub.3 are each independently nitrogen or a CH group, Y.sub.1 is a CH group, a CCl group, a CBr group or a CNH.sub.2 group, Y.sub.2 and Y.sub.3 are each independently nitrogen or a CH group, Y.sub.4 is hydrogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy or halogen, Y.sub.5 is NH.sub.2 or C.sub.1 -C.sub.4 alkoxy, Q is NH.sub.2, NHOH, NHCH.sub.3, OH, or hydrogen, and V is hydrogen, halogen or NH.sub.2 ; or a pharmaceutically acceptable salt thereof.

  本发明涉及一类新型的碳环衍生物，其化学式为(I)和(II)，并将其用作抗病毒和抗肿瘤药物，其中X1和X2各自独立地为氢、氟或氯，R为氢或羟甲基，J为式(a)、(b)和(c)的基团。Y1是一个CH基团、一个CCl基团、一个CBr基团或一个CNH2基团，Y2和Y3各自独立地为氮或一个CH基团，Y1是一个CH基团、一个CCl基团、一个CBr基团或一个CNH2基团，Y2和Y3各自独立地为氮或一个CH基团，Y4为氢、C1-C4烷基、C1-C4烷氧基或卤素，Y5为NH2或C1-C4烷氧基，Q为NH2、NHOH、NHCH3、OH或氢，V为氢、卤素或NH2；或其药学上可接受的盐。
• Benzene derivative
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：US11261154B2

  公开（公告）日：2022-03-01

  A compound represented by general formula (I) (in the formula, all symbols are as described in the description) or a salt thereof has a potent nerve-protecting and/or -repairing activity, and therefore can be used as a therapeutic agent for neuropathy (e.g., chronic inflammatory demyelinating polyneuropathy, Guillain-Barre syndrome, periarteritis nodosa, allergic vasculitis, diabetic peripheral neuropathy, entrapment neuropathy, peripheral neuropathy associated with the administration of a chemotherapeutic drug, or peripheral neuropathy associated with Charcot-Marie-Tooth disease).

  通式(I)代表的化合物（式中，所有符号均如说明中所描述）或其盐具有强效的神经保护和/或修复活性，因此可用作神经病变（如：慢性炎症性脱髓鞘性多发性神经病变、格林-巴利综合征、结节性动脉周围炎、过敏性血管炎、糖尿病周围神经病变、夹层神经病变、周围神经病变）的治疗剂、慢性炎症性脱髓鞘性多发性神经病、格林-巴利综合征、结节性动脉周围炎、过敏性血管炎、糖尿病周围神经病变、夹层神经病、与化疗药物相关的周围神经病变或与夏科-玛丽-牙病相关的周围神经病变）。
• Synthesis of aglycon analogues of sarmentosin and Their bioactivity of lymphocyte proliferation
  作者：Hong Zhang、Rui Xu、Zhongliang Hu、Xuchang He、Donglu Bai、Xiaoyu Li、Xiaofeng Wang

  DOI：10.1016/s0960-894x(02)00801-6

  日期：2002.12

  A number of aglycon analogues of sarmentosin were prepared and their bioactivities on the proliferation of T-lymphocytes and B-lymphocytes were assayed. (C) 2002 Elsevier Science Ltd. All rights reserved.