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methyl 6-methoxy-1-fluoro-1,2,3,4-tetrahydro-2-naphthylacetate

中文名称
——
中文别名
——
英文名称
methyl 6-methoxy-1-fluoro-1,2,3,4-tetrahydro-2-naphthylacetate
英文别名
methyl 2-(1-fluoro-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)acetate
methyl 6-methoxy-1-fluoro-1,2,3,4-tetrahydro-2-naphthylacetate化学式
CAS
——
化学式
C14H17FO3
mdl
——
分子量
252.286
InChiKey
BCKRJUIBRAYQTD-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):
    2.5
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    N,N-二乙基(2-氯-1,1,2-三氟乙基)胺 、 methyl 6-methoxy-1-hydroxy-1,2,3,4-tetrahydro-2-naphthylacetate 在 盐酸 作用下, 以 二氯甲烷 为溶剂, 生成 methyl 6-methoxy-1-fluoro-1,2,3,4-tetrahydro-2-naphthylacetate 、 6-methoxy-1,2-dihydro-2-naphthylacetate
    参考文献:
    名称:
    2-Naphthyl acetic acid derivatives and compositions and methods thereof
    摘要:
    2-萘乙酸衍生物及其相应的酰胺、酯、羟肟酸和其盐,可选择地在乙酸基团的α-位置和/或在萘环的位置6和/或在位置1、4、7或8处进行取代,并可选择地在位置3和4处饱和,具有抗炎、镇痛、退热和止痒作用。通过给予萘乙酸衍生物进行治疗炎症、疼痛、发热和瘙痒的药物方法。用于治疗上述疾病的药物组合物,包括萘乙酸衍生物。
    公开号:
    US03978116A1
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文献信息

  • 6-Substituted 2-naphthyl .alpha.-substituted acetamides
    申请人:Syntex Corporation
    公开号:US03978124A1
    公开(公告)日:1976-08-31
    2-Naphthyl acetic acid derivatives and the corresponding amides, esters, hydroxamic acids and addition salts thereof, optionally substituted at the .alpha.-position on the acetic acid moiety and/or at position 6 and/or at positions 1, 4, 7 or 8 on the naphthyl ring and optionally saturated at positions 3 and 4, are anti-inflammatory, analgesic, anti-pyretic and anti-pruritic agents. A pharmaceutical method of effecting treatment of inflammation, pain, pyrexia and pruritus by the administration of naphthyl acetic acid derivatives. A pharmaceutical composition for use in the treatment of the above maladies comprising a naphthyl acetic acid derivative.
    2-萘乙酸衍生物及其相应的酰胺、酯、羟肟酸和加成盐,可在乙酸基团的α-位置和/或在萘环的1、4、6、7或8位置上选择性地取代,并可在3和4位置上选择性地饱和。它们是抗炎、镇痛、退热和止痒剂。一种通过给予萘乙酸衍生物治疗炎症、疼痛、发热和瘙痒的药物方法。一种用于治疗上述疾病的药物组合物,包括萘乙酸衍生物。
  • 2-Naphthyl acetic acid derivatives
    申请人:Syntex Corporation
    公开号:US03980699A1
    公开(公告)日:1976-09-14
    2-Naphthyl acetic acid derivatives and the corresponding amides, esters, hydroxamic acids and addition salts thereof, optionally substituted at the .alpha.-position on the acetic acid moiety and/or at position 6 and/or at positions 1, 4, 7 or 8 on the naphthyl ring and optionally saturated at positions 3 and 4, are anti-inflammatory, analgesic, anti-pyretic and anti-pruritic agents. A pharmaceutical method of effecting treatment of inflammation, pain, pyrexia and pruritus by the administration of naphthyl acetic acid derivatives. A pharmaceutical composition for use in the treatment of the above maladies comprising a naphthyl acetic acid derivative.
    2-萘乙酸衍生物及其相应的酰胺、酯、羟肟酸和加成盐,可选择在乙酸基团的α-位置和/或在萘环的1、4、6、7或8号位上进行取代,可选择在3和4号位饱和,具有抗炎、镇痛、退热和止痒作用。一种通过给予萘乙酸衍生物来治疗炎症、疼痛、发热和瘙痒的药物方法。一种用于治疗上述疾病的药物组合物,包括萘乙酸衍生物。
  • Anti-inflammatory, analgesic, anti-pyretic and anti-pruritic
    申请人:Syntex Corporation
    公开号:US03998966A1
    公开(公告)日:1976-12-21
    2-Naphthyl acetic acid derivatives and the corresponding amides, esters, hydroxamic acids and addition salts thereof, optionally substituted at the .alpha.-position on the acetic acid moiety and/or at position 6 and/or at positions 1, 4, 7 or 8 on the naphthyl ring and optionally saturated at positions 3 and 4, are anti-inflammatory, analgesic, anti-pyretic and anti-pruritic agents. A pharmaceutical method of effecting treatment of inflammation, pain, pyrexia and pruritus by the administration of naphthyl acetic acid derivatives. A pharmaceutical composition for use in the treatment of the above maladies comprising a naphthyl acetic acid derivative.
    2-萘乙酸衍生物及其相应的酰胺、酯、羟肟酸和加成盐,在乙酸基团的α-位和/或萘环的1、4、6、7或8位可能被取代,且在3和4位可能被饱和,具有抗炎、镇痛、退热和止痒作用。使用萘乙酸衍生物的药物治疗方法,用于治疗炎症、疼痛、发热和瘙痒。一种用于治疗上述疾病的药物组合物,包括萘乙酸衍生物。
  • 6-Substituted 2-naphthyl acetic acid derivatives
    申请人:Syntex Corporation
    公开号:US04001301A1
    公开(公告)日:1977-01-04
    2-Naphthyl acetic acid derivatives and the corresponding amides, esters, hydroxamic acids and addition salts thereof, optionally substituted at the .alpha.-position on the acetic acid moiety and/or at position 6 and/or at positions 1, 4, 7 or 8 on the naphthyl ring and optionally saturated at positions 3 and 4, are anti-inflammatory, analgesic, antipyretic and anti-pruritic agents. A pharmaceutical method of effecting treatment of inflammation, pain, pyrexia and pruritus by the administration of naphthyl acetic acid derivatives. A pharmaceutical composition for use in the treatment of the above maladies comprising a naphthyl acetic acid derivative.
    2-萘乙酸衍生物及其相应的酰胺、酯、羟肟酸和加成盐,可选地在乙酸基团的α-位置和/或在萘环的1、4、6、7或8号位置取代,并可选地在3号和4号位置饱和,具有抗炎、镇痛、退热和抗瘙痒作用。一种通过给予萘乙酸衍生物治疗炎症、疼痛、发热和瘙痒的药物方法。一种用于治疗上述疾病的药物组合物,包括萘乙酸衍生物。
  • 2-Naphthylacetic acid derivatives and compositions and methods thereof
    申请人:Syntex Corporation
    公开号:US04051233A1
    公开(公告)日:1977-09-27
    2-Naphthyl acetic acid derivatives and the corresponding amides, esters, hydroxamic acids and addition salts thereof, optionally substituted at the .alpha.-position on the acetic acid moiety and/or at position 6 and/or at positions 1, 4, 7 or 8 on the naphthyl ring and optionally saturated at positions 3 and 4, are anti-inflammatory, analgesic, anti-pyretic and anti-pruritic agents. A pharmaceutical method of effecting treatment of inflammation, pain, pyrexia and pruritus by the administration of naphthyl acetic acid derivatives. A pharmaceutical composition for use in the treatment of the above maladies comprising a naphthyl acetic acid derivative.
    2-萘乙酸衍生物及其相应的酰胺、酯、羟肟酸和加成盐,可选择性地在乙酸基团的α-位置和/或萘环的1、4、6、7或8位置进行取代,并可选择性地在3和4位置饱和,具有抗炎、镇痛、退热和抗瘙痒作用。一种利用萘乙酸衍生物进行治疗炎症、疼痛、发热和瘙痒的药物方法。一种用于治疗上述疾病的药物组合物,包括萘乙酸衍生物。
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