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2-ethoxy-1,3-dioxolane-4(R),5(R)-dimethanol | 95532-12-0

中文名称
——
中文别名
——
英文名称
2-ethoxy-1,3-dioxolane-4(R),5(R)-dimethanol
英文别名
((4R,5R)-2-ethoxy-1,3-dioxolane-4,5-diyl)dimethanol;[(4R,5R)-2-ethoxy-5-(hydroxymethyl)-1,3-dioxolan-4-yl]methanol
2-ethoxy-1,3-dioxolane-4(R),5(R)-dimethanol化学式
CAS
95532-12-0
化学式
C7H14O5
mdl
——
分子量
178.185
InChiKey
MOAWDMIKGNZSQA-PHDIDXHHSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    301.7±37.0 °C(Predicted)
  • 密度:
    1.25±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.1
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    68.2
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-ethoxy-1,3-dioxolane-4(R),5(R)-dimethanol五氯化磷 、 sodium hydride 作用下, 以 四氢呋喃二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 生成 (2R,3S)-1,4-bis(benzyloxy)-3-chlorobutan-2-yl formate
    参考文献:
    名称:
    [EN] PROCESSES FOR THE PREPARATION OF ARGINASE INHIBITORS AND THEIR SYNTHETIC INTERMEDIATES
    [FR] PROCÉDÉS DE PRÉPARATION D'INHIBITEURS D'ARGINASE ET LEURS INTERMÉDIAIRES SYNTHÉTIQUES
    摘要:
    本文提供了用于制备某些化合物的过程和中间体,包括公式21或公式22的化合物,或者两者中任何一个的药用可接受盐。
    公开号:
    WO2022016195A1
  • 作为产物:
    描述:
    diethyl D-tartrate, cyclic ethyl orthoformate 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 生成 2-ethoxy-1,3-dioxolane-4(R),5(R)-dimethanol
    参考文献:
    名称:
    [EN] PROCESSES FOR THE PREPARATION OF ARGINASE INHIBITORS AND THEIR SYNTHETIC INTERMEDIATES
    [FR] PROCÉDÉS DE PRÉPARATION D'INHIBITEURS D'ARGINASE ET LEURS INTERMÉDIAIRES SYNTHÉTIQUES
    摘要:
    本文提供了用于制备某些化合物的过程和中间体,包括公式21或公式22的化合物,或者两者中任何一个的药用可接受盐。
    公开号:
    WO2022016195A1
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文献信息

  • Phenolic antioxidants for the treatment of disorders including arthritis, asthma and coronary artery disease
    申请人:Meng Q. Charles
    公开号:US20060020038A1
    公开(公告)日:2006-01-26
    The invention relates to compounds, pharmaceutical compositions comprising the compounds, and methods of using the compounds, wherein the compounds are of the following Formulas: or a pharmaceutically acceptable salt, ester or prodrug thereof, wherein the substituents are defined in the application. The invention further provides methods of treatment of inflammatory disorders by administering the compounds.
    本发明涉及化合物、包含该化合物的药物组成物以及使用该化合物的方法,其中该化合物的结构式为:或其药学上可接受的盐、酯或前药,其中取代基在申请中有定义。本发明进一步提供通过给予该化合物治疗炎症性疾病的方法。
  • Total synthesis of ionophore antibiotic X-14547A
    作者:K. C. Nicolaou、D. P. Papahatjis、D. A. Claremon、R. L. Magolda、R. E. Dolle
    DOI:10.1021/jo00209a017
    日期:1985.5
  • Discovery of Novel Phenolic Antioxidants as Inhibitors of Vascular Cell Adhesion Molecule-1 Expression for Use in Chronic Inflammatory Diseases
    作者:Charles Q. Meng、Patricia K. Somers、Lee K. Hoong、X. Sharon Zheng、Zhihong Ye、Kimberly J. Worsencroft、Jacob E. Simpson、Martha R. Hotema、M. David Weingarten、Mathew L. MacDonald、Russell R. Hill、Elaine M. Marino、Ki-Ling Suen、Jayraz Luchoomun、Charles Kunsch、Laura K. Landers、Dimitria Stefanopoulos、Randy B. Howard、Cynthia L. Sundell、Uday Saxena、Martin A. Wasserman、James A. Sikorski
    DOI:10.1021/jm049685u
    日期:2004.12.1
    Vascular cell adhesion molecule-1 (VCAM-1) mediates recruitment of leukocytes to endothelial cells and is implicated in many inflammatory conditions. Since part of the signal transduction pathway that regulates the activation of VCAM-1 expression is redox-sensitive, compounds with antioxidant properties may have inhibitory effects on VCAM-1 expression. Novel phenolic compounds have been designed and synthesized starting from probucol (1). Many of these compounds demonstrated potent inhibitory effects on cytokine-induced VCAM-1 expression and displayed potent antioxidant effects in. vitro. Some of these derivatives (4o, 4p, 4w, and 4x) inhibited lipopolysaccharide (LPS)-induced secretion of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), and IL-6 from human peripheral blood mononuclear cells (hPBMCs) in a concentration-dependent manner in vitro and showed antiinflammatory effects in an animal model. Compounds 4ad and 4ae are currently in clinical trials for the treatment of rheumatoid arthritis (RA) and prevention of chronic organ transplant rejection, respectively.
  • US7271274B2
    申请人:——
    公开号:US7271274B2
    公开(公告)日:2007-09-18
  • [EN] PHENOLIC ANTIOXIDANTS FOR THE TREATMENT OF DISORDERS INCLUDING ARTHRITIS, ASTHMA AND CORONARY ARTERY DISEASE<br/>[FR] ANTIOXYDANTS PHÉNOLIQUES POUR LE TRAITEMENT DE TROUBLES INCLUANT L'ARTHRITE, L'ASTHME ET LES TROUBLES DES ARTÈRES CORONAIRES
    申请人:ATHEROGENICS INC
    公开号:WO2005112914A2
    公开(公告)日:2005-12-01
    The invention relates to compounds, pharmaceutical compositions comprising the compounds, and methods of using the compounds, wherein the compounds are of the following Formulas: or a pharmaceutically acceptable salt, ester or prodrug thereof, wherein the substituents are defined in the application. The invention further provides methods of treatment of inflammatory disorders by administering the compounds.
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