摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2,4-dihydroxy-[1]naphthoic acid ethyl ester | 58380-29-3

中文名称
——
中文别名
——
英文名称
2,4-dihydroxy-[1]naphthoic acid ethyl ester
英文别名
2,4-Dihydroxy-[1]naphthoesaeure-aethylester;ethyl 2,4-dihydroxy-1-naphthoate;ethyl-2,4-dihydroxy-1-naphthoate;ethyl 2,4-dihydroxynaphthalene-1-carboxylate
2,4-dihydroxy-[1]naphthoic acid ethyl ester化学式
CAS
58380-29-3
化学式
C13H12O4
mdl
——
分子量
232.236
InChiKey
YGYIORPHKFQKSV-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

物化性质

  • 熔点:
    137-138 °C
  • 沸点:
    446.6±15.0 °C(Predicted)
  • 密度:
    1.328±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

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

点击查看最新优质反应信息

文献信息

  • Photochromic naphthopyrans
    申请人:PPG Industries Ohio, Inc.
    公开号:US06353102B1
    公开(公告)日:2002-03-05
    Described are novel photochromic naphtho[1,2-b]pyran compounds having certain substituents at the 2 position of the pyran ring, certain substituents at the 5 and 6 positions and optionally at the 7, 8, 9 and 10-positions of the naphtho portion of the compound. These compounds may be represented by the following graphic formula: Also described are polymeric organic host materials that contain or that are coated with such compounds. Optically clear articles such as ophthalmic lenses or contact lenses that incorporate the novel naphthopyran compounds or combinations thereof with complementary photochromic compounds, e.g., certain other naphthopyrans, benzopyrans, and spiro(indoline)type compounds, are also described.
    描述了具有萘并[1,2-b]吡喃环2位具有特定取代基,5位和6位以及化合物的萘部分的7、8、9和10位位置可选地具有特定取代基的新型光致变色萘[1,2-b]吡喃化合物。这些化合物可以用以下图式表示: 还描述了含有或涂有这些化合物的聚合有机宿主材料。还描述了包含新型萘吡喃化合物或其与互补光致变色化合物(例如,某些其他萘吡喃、苯并吡喃和螺(indoline)型化合物)的组合的光学透明物品,例如眼镜或隐形眼镜。
  • [EN] NAPHTHALENECARBOXAMIDES AS TACHYKININ RECEPTOR ANTAGONISTS<br/>[FR] NAPHTALENE-CARBOXAMIDES UTILISES EN TANT QU'ANTAGONISTES DES RECEPTEURS DES TACHYKININES
    申请人:ZENECA LTD
    公开号:WO2000020389A1
    公开(公告)日:2000-04-13
    A compound having formula (I) wherein R1 is oxo, -ORa, -OC(=O)Rb; or (A); R2 is H; or R?1 is -ORc and R2 is -ORd; or R1 and R2¿ together form -O(CH¿2?)mO-; and any pharmaceutically-acceptable salt thereof along with their use in treating depression, anxiety, asthma, rheumatoid arthritis, Alzheimer's disease, cancer, schizophrenia, oedema, allergic rhinitis, inflammation, pain, gastrointestinal-hypermotility, anxiety, emesis, Huntington's disease, psychoses including depression, hypertension, migraine, bladder hypermotility, or urticaria, along with methods of making the compounds and pharmaceutical compositions containing the compounds.
    化合物式(I)的化合物,其中R1是氧代、-ORa、-OC(=O)Rb;或(A);R2是H;或者R1是-ORc且R2是-ORd;或者R1和R2在一起形成-O(CH2)mO-;以及其任何药学上可接受的盐,用于治疗抑郁症、焦虑症、哮喘、类风湿性关节炎、阿尔茨海默病、癌症、精神分裂症、水肿、过敏性鼻炎、炎症、疼痛、胃肠过度运动、焦虑症、呕吐、亨廷顿病、包括抑郁症、高血压、偏头痛、膀胱过度运动或荨麻疹的方法,以及制备这些化合物和含有这些化合物的制药组合物。
  • Naphthalenecarboxamides as tachykinin receptor antagonists
    申请人:AstraZeneca AB
    公开号:EP1433783A2
    公开(公告)日:2004-06-30
    A compound having the formula (I) wherein R1 is oxo, -ORa, -OC(=O)Rb; or (A); R2 is H; or R1 is -ORc and R2 is -ORd; or R1 and R2 together form -O(CH2)mO-; R3 is H or alkyl; R4, R5 and R6 are independently selected from hydroxy, cyano, nitro, trifluoromethoxy, trifluoromethyl, alkylsulfonyl, halo, alkoxy, alkyl, cyanoalkyl, alkenyl, alkynyl, carboxy, alkoxy-carbonyl, carbamoyl, alkylcarbamoyl, di-alkylcarbamoyl, alkanoyl, alkanoylamino, aminosulfonyl, and substituted alkyl; or R4 and R5 together form -OCH2O- or -OC(CH3)2O-; R6 may additionally be hydrogen; R7 is substituted phenyl; R8 is selected from hydrogen, hydroxy, alkoxy, alkanoyloxy, alkanoyl, alkoxycarbonyl, alkanoylamino, alkyl, carbamoyl, alkylcarbamoyl, and bis(alkyl)carbamoyl; Ra is hydrogen or alkyl; Rb is alkyl, aryl or arylalkyl; Rc and Rd are independently selected from alkyl; m is 2, 3, or 4; and X1 and X2 are independently H or halogen, wherein at least one of X1 and X2 are halogen; and any pharmaceutically-acceptable salt thereof along with their use in treating depression, anxiety, asthma, rheumatoid arthritis, Alzheimer's disease, cancer, schizophrenia, oedema, allergic rhinitis, inflammation, pain, gastrointestinal-hypermotility, anxiety, emesis, Huntington's disease, psychoses including depression, hypertension, migraine, bladder hypermotility, or urticaria, along with methods of making the compounds and pharmaceutical compositions containing the compounds.
    具有式 (I) 的化合物 其中 R1 是氧代、-ORa、-OC(=O)Rb;或 (A); R2 是 H;或 R1 是-ORc,R2 是-ORd;或 R1 和 R2 共同形成-O(CH2)mO-; R3 是 H 或烷基;R4、R5 和 R6 独立选自羟基、氰基、硝基、三氟甲氧基、三氟甲基、烷基磺酰基、卤代、烷氧基、烷基、氰基烷基、烯基、炔基、羧基、烷氧基羰基、氨基甲酰基、烷基氨基甲酰基、二烷基氨基甲酰基、烷酰基、烷酰氨基、氨基磺酰基和取代烷基;或 R4 和 R5 共同形成 -OCH2O- 或 -OC(CH3)2O-;R6 还可以是氢;R7 是取代的苯基;R8 选自氢、羟基、烷氧基、烷酰氧基、烷酰基、烷氧羰基、烷酰氨基、烷基、氨基甲酰基、烷基氨基甲酰基和双(烷基)氨基甲酰基;Ra 是氢或烷基;Rb 是烷基、芳基或芳烷基;Rc 和 Rd 独立地选自烷基;m 是 2、3 或 4;以及 X1 和 X2 独立地是 H 或卤素,其中 X1 和 X2 中至少有一个是卤素;及其任何药学上可接受的盐,以及它们在治疗抑郁症、焦虑症、哮喘、类风湿性关节炎、阿尔茨海默病、癌症、精神分裂症、水肿、过敏性鼻炎、炎症、疼痛、胃肠道过度运动、焦虑症、呃逆、亨廷顿氏病、包括抑郁症在内的精神病、高血压、偏头痛、膀胱过度运动或荨麻疹中的用途,以及制造这些化合物和含有这些化合物的药物组合物的方法。
  • Neunhoeffer; v. Hoerner, Chemische Berichte, 1950, vol. 83, p. 99,103
    作者:Neunhoeffer、v. Hoerner
    DOI:——
    日期:——
  • BRUGGINK A.; MCKILLOP A., TETRAHEDRON <TETR-AB>, 1975, 31, NO 20, 2607-2619
    作者:BRUGGINK A.、 MCKILLOP A.
    DOI:——
    日期:——
查看更多