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8-methoxy-2H-chromene-4-carboxylic acid | 853926-28-0

中文名称
——
中文别名
——
英文名称
8-methoxy-2H-chromene-4-carboxylic acid
英文别名
8-Methoxy-2H-chromen-4-carbonsaeure;8-methoxy-2H-chromene-4-carboxylic acid
8-methoxy-2<i>H</i>-chromene-4-carboxylic acid化学式
CAS
853926-28-0
化学式
C11H10O4
mdl
——
分子量
206.198
InChiKey
LADJUCSRSKGMSA-UHFFFAOYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    8-methoxy-2H-chromene-4-carboxylic acid吡啶氢氟酸 作用下, 生成 (2,4-diacetoxy-3-isopentyl-phenyl)-(8-methoxy-2H-chromen-4-yl)-ketone
    参考文献:
    名称:
    Offe; Barkow, Chemische Berichte, 1947, vol. 80, p. 464,467
    摘要:
    DOI:
  • 作为产物:
    描述:
    8-methoxy-3-oxo-chroman-4-carboxylic acid ethyl ester 在 氢氧化钾乙醇 作用下, 生成 8-methoxy-2H-chromene-4-carboxylic acid
    参考文献:
    名称:
    O'Donnell et al., Journal of the Chemical Society, 1936, p. 419,422
    摘要:
    DOI:
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文献信息

  • AMIDES AS 11-BETA HYDROXYSTEROID DEHYDROGENASE INHIBITORS
    申请人:Janssen Pharmaceutica NV
    公开号:EP1581476B1
    公开(公告)日:2016-11-16
  • ADAMANTYL ACETAMIDES AS 11-BETA HYDROXYSTEROID DEHYDROGENASE INHIBITORS
    申请人:Linders Theodorus Maria Joannes
    公开号:US20080096869A1
    公开(公告)日:2008-04-24
    the N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein n represents an integer being 1 or 2; R 1 and R 2 each independently represents hydrogen C 1-4 alkyl, NR 9 R 10 , C 1-4 alkyloxy; or R 1 and R 2 taken together with the carbon atom with which they are attached form a C 3-6 cycloalkyl; and where n is 2, either R 1 or R 2 may be absent to form an unsaturated bond; R 3 represents a C 6-12 cycloalkyl, preferably selected from cylo-octanyl and cyclohexyl or R 3 represents a monovalent radical having one of the following formulae wherein said C 6-12 cycloalkyl or monovalent radical may optionally be substituted with one, or where possible two, three or more substituents selected from the group consisting of C 1-4 alkyl, C 1-4 alkyloxy, halo or hydroxy; Q represents Het 1 or Ar 2 wherein said C 3-8 cycloalkyl, Het 1 or Ar 2 are optionally substituted with one or where possible two or more substituents selected from halo, C 1-4 alkyl, C 1-4 alkyloxy, hydroxy, nitro, NR 5 R 6 , C 1-4 alkyloxy substituted with one or where possible two, three or more substituents each independently selected from hydroxycarbonyl, Het 2 and NR 7 R 8 , and C 1-4 alkyl substituted with one or where possible two or three halo substituents, preferably trifluoromethyl; R 5 and R 6 each independently represent hydrogen, C 1-4 alkyl, or C 1-4 alkyl substituted with phenyl; R 7 and R 8 each independently represent hydrogen or C 1-4 alkyl; R 9 and R 10 each independently represent hydrogen, C 1-4 alkyl or C 1-4 alkyloxycarbonyl; L represents C 1-4 alkyl; Het 1 represents a heterocycle selected from pyridinyl, thiophenyl, or 1,3-benzodioxolyl; Het 2 represents piperidinyl, pyrrolidinyl or morpholinyl; Ar 2 represents phenyl, naphtyl or indenyl.
  • US7332524B2
    申请人:——
    公开号:US7332524B2
    公开(公告)日:2008-02-19
  • US7968601B2
    申请人:——
    公开号:US7968601B2
    公开(公告)日:2011-06-28
  • Offe; Barkow, Chemische Berichte, 1947, vol. 80, p. 464,467
    作者:Offe、Barkow
    DOI:——
    日期:——
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