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4-氯-2-萘酚 | 75907-51-6

中文名称
4-氯-2-萘酚
中文别名
——
英文名称
4-chloro-2-naphthol
英文别名
1-Chloro-3-hydroxynaphthalene;4-chloronaphthalen-2-ol
4-氯-2-萘酚化学式
CAS
75907-51-6
化学式
C10H7ClO
mdl
MFCD01712262
分子量
178.618
InChiKey
FPBMWSBRLLFCEG-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:
    100 °C
  • 沸点:
    327.2±15.0 °C(Predicted)
  • 密度:
    1.333±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    4-氯-2-萘酚potassium tert-butylatepotassium carbonate 作用下, 以 四氢呋喃丙酮 为溶剂, 生成
    参考文献:
    名称:
    路易斯与苯酚介导的烯烃分子内三氟甲基硫醇化:获得含SCF3的铬烷和二氢苯并呋喃化合物。
    摘要:
    首次公开了路易斯酸介导的烯烃与酚的分子内三氟甲基硫醇化,该酚可以直接进入含SCF 3的苯并二氢呋喃和二氢苯并呋喃化合物。使用γ-取代的2-烯丙基苯酚作为底物,以中等至良好的产率获得了许多含SCF 3的苯并二氢吡喃。同时,还使用β-取代的2-烯丙基酚作为底物以中等至良好的产率递送了具有氧杂-季中心的各种含SCF 3的二氢苯并呋喃。
    DOI:
    10.1021/acs.orglett.0c02744
  • 作为产物:
    描述:
    1,4-二氯-[2]萘酚 在 tin(ll) chloride 作用下, 以 溶剂黄146 为溶剂, 生成 4-氯-2-萘酚
    参考文献:
    名称:
    Repinskaya, I. B.; Savel'ev, V. A.; Makarova, Z. S., Journal of Organic Chemistry USSR (English Translation), 1980, p. 1463 - 1466
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • [EN] TETRAZOLINONE COMPOUNDS AND ITS USE AS PESTICIDES<br/>[FR] COMPOSÉS DE TÉTRAZOLINONE ET LEUR UTILISATION EN TANT QUE PESTICIDES
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2013162072A1
    公开(公告)日:2013-10-31
    The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc., which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc.; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc.; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc.; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.
    本发明提供了一种具有优异杀虫效果的化合物。公式(1)的四唑酮化合物:[其中R1代表C6-C16芳基、C1-C12烷基或C3-C12环烷基等,每个都可以选择性地被取代;R2、R3、R4和R5分别独立地代表氢原子、卤素原子或C1-C3烷基等;R6代表C1-C6烷基、C3-C6环烷基、卤素原子、C1-C6卤代烷基、C2-C6烯基、C1-C6烷氧基或C1-C6卤代烷氧基等;R7、R8和R9分别独立地代表氢原子、卤素原子或C1-C4烷基等;X代表氧原子或硫原子;R10代表C1-C6烷基等]在杀虫方面表现出优异的控制效果。
  • Synthesis, Biological Activity Evaluation and Molecular Modeling Study on the New Isoconessimine Derivatives as Acetylcholinesterase Inhibitors
    作者:Guofei Jin、Zhongduo Yang、Weiwei Xue、Jie Sheng、Yin Shi、Xiaojun Yao
    DOI:10.1002/cjoc.201300441
    日期:2013.9
    110 nmol/L which is close to that of reference compound huperzine A (IC50=70 nmol/L). The mode of AChE inhibition by 7b was reversible and non‐competitive. In addition, molecular modeling was performed to explore the binding mode of inhibitor 7b at the active site of AChE and the results showed that 7b could be docked into the acetylcholinesterase active site and compound 7b had hydrophobic interactions
    新的异cosnessimine衍生物是从conessine(1)合成的,并被评估为乙酰胆碱酯酶(AChE)抑制剂。衍生物是通过两个反应步骤(N-去甲基化和亲核取代)制备的。所有合成的衍生物均显示出比Conessine(1)(IC 50 = 16 µmol·L -1)和异椰油亚胺(2)(IC 50 > 300 µmol·L -1)更高的潜在抗乙酰胆碱酯酶活性。化合物7b(3β- [甲基-[2- [4-(4-硝基苯氧基)乙基]氨基] con-5-烯酸)对IC 50的抑制作用最强110 nmol / L的浓度接近参考化合物石杉碱A的浓度(IC 50 = 70 nmol / L)。7b抑制AChE的模式是可逆的,并且是非竞争性的。此外,进行分子建模以探索抑制剂7b在AChE活性位点的结合方式,结果表明7b可以与乙酰胆碱酯酶活性位点对接,化合物7b与Trp279和Leu282发生疏水相互作用。
  • [EN] TETRAZOLINONE COMPOUNDS AND ITS USE<br/>[FR] COMPOSÉS DE TÉTRAZOLINONE ET LEUR UTILISATION
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2013162077A1
    公开(公告)日:2013-10-31
    The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein, R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, a C3-C12 cycloalkyl group or an adamantyl group, etc., which each optionally be substituted; R2 represents a hydrogen atom, an C1-C12 alkyl group, or a halogen atom, etc.; R4 and R5 represent independently of each other a hydrogen atom or an C1-C3 alkyl group, etc.; R6, R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, an C1-C12 alkyl group, a C1-C12 haloalkyl group, an C2-C12 alkenyl group, a C3-C12 cycloalkyl group, an C1-C12 alkoxy group or a C1-C12 haloalkoxy group, etc.; X and Y represent independently of each other a sulfur atom or an oxygen atom; Q represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.
    本发明提供了一种具有优异杀虫效果的化合物。式(1)中的四氮杂酮化合物:[其中,R1代表一个C6-C16芳基,一个C1-C12烷基,一个C3-C12环烷基或一个金刚烷基等,每个都可以选择性地被取代;R2代表一个氢原子,一个C1-C12烷基或一个卤素原子等;R4和R5分别独立地代表一个氢原子或一个C1-C3烷基等;R6、R7、R8和R9分别独立地代表一个氢原子,一个卤素原子,一个C1-C12烷基,一个C1-C12卤代烷基,一个C2-C12烯基,一个C3-C12环烷基,一个C1-C12烷氧基或一个C1-C12卤代烷氧基等;X和Y分别独立地代表一个硫原子或一个氧原子;Q代表一个氧原子或一个硫原子;R10代表一个C1-C6烷基等]对害虫有极佳的控制效果。
  • TETRAZOLINONE COMPOUNDS AND ITS USE
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:US20150031733A1
    公开(公告)日:2015-01-29
    The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein, R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, a C3-C12 cycloalkyl group or an adamantyl group, etc., which each optionally be substituted; R2 represents a hydrogen atom, an C1-C12 alkyl group, or a halogen atom, etc.; R4 and R5 represent independently of each other a hydrogen atom or an C1-C3 alkyl group, etc.; R6, R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, an C1-C12 alkyl group, a C1-C12 haloalkyl group, an C2-C12 alkenyl group, a C3-C12 cycloalkyl group, an C1-C12 alkoxy group or a C1-C12 haloalkoxy group, etc.; X and Y represent independently of each other a sulfur atom or an oxygen atom; Q represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.
    本发明提供了一种具有优异的杀虫功效的化合物。公式(1)的四唑酮化合物:[其中,R1代表C6-C16芳基,C1-C12烷基,C3-C12环烷基或金刚烷基等,每个都可以选择性地被取代;R2代表氢原子,C1-C12烷基或卤素原子等;R4和R5分别独立地代表氢原子或C1-C3烷基等;R6、R7、R8和R9分别独立地代表氢原子、卤素原子、C1-C12烷基、C1-C12卤代烷基、C2-C12烯基、C3-C12环烷基、C1-C12烷氧基或C1-C12卤代烷氧基等;X和Y分别独立地代表硫原子或氧原子;Q代表氧原子或硫原子;R10代表C1-C6烷基等]在控制害虫方面表现出优异的效果。
  • TETRAZOLINONE COMPOUNDS AND ITS USE AS PESTICIDES
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:US20150051171A1
    公开(公告)日:2015-02-19
    The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc., which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc.; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc.; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc.; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.
    本发明提供了一种具有优异的杀虫功效的化合物。公式(1)的四唑烷酮化合物:[其中,R1代表C6-C16芳基,C1-C12烷基或C3-C12环烷基等,每个都可以选择性地被取代;R2、R3、R4和R5分别独立地表示氢原子、卤素原子或C1-C3烷基等;R6表示C1-C6烷基,C3-C6环烷基,卤素原子,C1-C6卤代烷基,C2-C6烯基,C1-C6烷氧基或C1-C6卤代烷氧基等;R7、R8和R9独立地表示氢原子、卤素原子或C1-C4烷基等;X表示氧原子或硫原子;R10表示C1-C6烷基等]对害虫具有优异的控制功效。
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