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6-nitro-2-methoxymethyl-2,5,7,8-tetramethyl-(2H)-chromene | 784163-74-2

中文名称
——
中文别名
——
英文名称
6-nitro-2-methoxymethyl-2,5,7,8-tetramethyl-(2H)-chromene
英文别名
6-nitro-2-methoxymethyl-2,5,7,8-tetramethyl-2H-chroman;6-nitro-2-methoxymethyl-2,5,7,8-tetramethyl (2H) chromene;2-(methoxymethyl)-2,5,7,8-tetramethyl-6-nitrochromene
6-nitro-2-methoxymethyl-2,5,7,8-tetramethyl-(2H)-chromene化学式
CAS
784163-74-2
化学式
C15H19NO4
mdl
——
分子量
277.32
InChiKey
FTEPOBOUBVEGAQ-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):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    64.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Phenylazole compounds production process and antioxidants
    申请人:Umeda Nobuhiro
    公开号:US20060247228A1
    公开(公告)日:2006-11-02
    The present invention is directed to compounds represented by the formula (1): B-D-Z  (1) [wherein B represent the following formula (B-1), (B-2) or (B-3); A represents an optionally substituted imidazole or pyrazole group; E represents the following formula (1a): X represents an oxygen atom, the formula: SOu, or the formula: N—R 9 ; Y represents a carbon atom or a nitrogen atom; D represents an oxygen atom, a sulfur atom or the formula (1a); Z represents (a chroman-2-yl group, a chroman-4-yl group, a 2,3-dihydrobenzofuran-2-yl group, a 2,3-dihydrobenzofuran-3-yl group, etc.) which is substituted with NHR 10 or OR 11 )] or pharmaceutically acceptable salts thereof, and to antioxidants, therapeutic agents for kidney diseases or cerebrovascular disorder, and retinal oxidative damage inhibitors, which include the compounds as the active ingredient.
    本发明涉及由式(1)表示的化合物:B-D-Z  (1)[其中B代表以下式(B-1),(B-2)或(B-3);A代表可选取代的咪唑吡唑基团;E代表以下式(1a):X代表氧原子,式:SOu或式:N-R9; Y代表碳原子或氮原子;D代表氧原子、原子或式(1a);Z代表(取代NHR10或OR11的香豆素-2-基基团、香豆素-4-基基团、2,3-二氢苯并呋喃-2-基基团、2,3-二氢苯并呋喃-3-基基团等)或其药学上可接受的盐,并且包括这些化合物作为活性成分的抗氧化剂、肾脏疾病或脑血管障碍治疗剂和视网膜氧化损伤抑制剂
  • PHENYLAZOLE COMPOUNDS, PRODUCTION PROCESS AND ANTIOXIDANTS
    申请人:Umeda Nobuhiro
    公开号:US20090306055A1
    公开(公告)日:2009-12-10
    The present invention is directed to compounds represented by the formula (1): B-D-Z (1), wherein B represent the following formula (B-1), A represents an optionally substituted imidazole or pyrazole group; E represents the following formula (1a): X represents an oxygen atom, the formula: SOu, or the formula: N—R 9 ; Y represents a carbon atom or a nitrogen atom; D represents an oxygen atom, a sulfur atom or the formula (1a); Z represents (a chroman-2-yl group, a chroman-4-yl group, a 2,3-dihydrobenzofuran-2-yl group, a 2,3-dihydrobenzofuran-3-yl group, etc.) which is substituted with NHR 10 or OR 11 )] or pharmaceutically acceptable salts thereof, and to antioxidants, therapeutic agents for kidney diseases or cerebrovascular disorder, and retinal oxidative damage inhibitors, which include the compounds as the active ingredient.
    本发明涉及由式(1)表示的化合物:B-D-Z(1),其中B代表以下式(B-1),A代表可选取代的咪唑吡唑基团;E代表以下式(1a):X代表氧原子,式:SOu,或式:N—R9;Y代表碳原子或氮原子;D代表氧原子、原子或式(1a);Z代表(一个被NHR10或OR11取代的2-色基基团、4-色基基团、2,3-二氢苯并呋喃-2-基基团、2,3-二氢苯并呋喃-3-基基团等)或其药学上可接受的盐,以及将该化合物作为活性成分的抗氧化剂、肾脏疾病或脑血管疾病的治疗剂和视网膜氧化损伤抑制剂
  • EP1650206
    申请人:——
    公开号:——
    公开(公告)日:——
  • US7553837B2
    申请人:——
    公开号:US7553837B2
    公开(公告)日:2009-06-30
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