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N,N-二丁基-4-己氧基-1-萘脒 | 3748-77-4

中文名称
N,N-二丁基-4-己氧基-1-萘脒
中文别名
丁萘脒; N,N-二丁基-4-己氧基-1-萘脒
英文名称
N,N-Dibutyl-4-hexyloxy-<1>naphthamidin
英文别名
bunamidine;N,N-dibutyl-4-hexoxynaphthalene-1-carboximidamide
N,N-二丁基-4-己氧基-1-萘脒化学式
CAS
3748-77-4
化学式
C25H38N2O
mdl
——
分子量
382.59
InChiKey
FGGFIMIICGZCCJ-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:
    214.0-214.8 °C
  • 沸点:
    495.0±47.0 °C(Predicted)
  • 密度:
    0.98

计算性质

  • 辛醇/水分配系数(LogP):
    7.5
  • 重原子数:
    28
  • 可旋转键数:
    14
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    36.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2925290090

反应信息

  • 作为反应物:
    描述:
    硝碘酚腈N,N-二丁基-4-己氧基-1-萘脒 生成 N,N-dibutyl-4-hexoxynaphthalene-1-carboximidamide;4-hydroxy-3-iodo-5-nitrobenzonitrile
    参考文献:
    名称:
    SCHAWARTZ, J.;DAVID, A.;HORVATH, G.
    摘要:
    DOI:
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文献信息

  • [EN] AZIRIDINE SPINOSYN DERIVATIVES AND METHODS OF MAKING<br/>[FR] DÉRIVÉS D'AZIRIDINE SPINOSYNE ET LEURS PROCÉDÉS DE FABRICATION
    申请人:AGRIMETIS LLC
    公开号:WO2018132288A1
    公开(公告)日:2018-07-19
    Compositions including derivatives of spinosyns of the following formulae and methods for the production of derivatives of spinosyns are provided. The spinosyn derivatives described herein include those functionalized on the C-5,6 double bond to provide an aziridine ring system. The method produces spinosyn derivatives that exhibit activity towards insects, arachnids, and nematodes and are useful in the agricultural and animal health markets.
    提供了包括以下公式的自旋菌素衍生物的组合物,以及用于生产自旋菌素衍生物的方法。本文描述的自旋菌素衍生物包括在C-5,6双键上官能化以提供环氮丙烷环系统的衍生物。该方法生产出对昆虫、蜘蛛和线虫具有活性的自旋菌素衍生物,并在农业和动物健康市场中有用。
  • ANTHELMINTIC COMPOUNDS AND COMPOSITIONS AND METHOD OF USING THEREOF
    申请人:Meng Charles Q.
    公开号:US20140142114A1
    公开(公告)日:2014-05-22
    The present invention relates to novel anthelmintic compounds of formula (I) below: wherein Y and Z are independently a bicyclic carbocyclic or a bicyclic heterocyclic group, or one of Y or Z is a bicyclic carbocyclic or a bicyclic heterocyclic group and the other of Y or Z is alkyl, alkenyl, alkynyl, cycloalkyl, phenyl, heterocyclyl or heteroaryl, and variables X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 are as defined herein. The invention also provides for veterinary compositions comprising the anthelmintic compounds of the invention, and their uses for the treatment and prevention of parasitic infections in animals.
    本发明涉及以下式(I)的新型驱虫化合物: 其中 Y和Z分别是双环碳环或双环杂环基团,或者Y或Z中的一个是双环碳环或双环杂环基团,另一个是烷基,烯基,炔基,环烷基,苯基,杂环基或杂芳基,以及变量X 1 ,X 2 ,X 3 ,X 4 ,X 5 ,X 6 ,X 7 和X 8 如本文所定义。本发明还提供了包含本发明的驱虫化合物的兽药组合物,以及它们用于治疗和预防动物寄生虫感染的用途。
  • [EN] ANTHELMINTIC DEPSIPEPTIDE COMPOUNDS<br/>[FR] COMPOSÉS DEPSIPEPTIDIQUES ANTHELMINTHIQUES
    申请人:MERIAL INC
    公开号:WO2018093920A1
    公开(公告)日:2018-05-24
    The present invention provides cyclic depsipeptide compounds of formula (I) wherein the stereochemical configuration of at least one carbon atom bearing the groups Cy1, Cy2, R1, R2, R3, R4, Ra and Rb is inverted compared with the naturally occurring cyclic depsipeptide PF1022A. The invention also provides compositions comprising the compounds that are effective against parasites that harm animals. The compounds and compositions may be used for combating parasites in or on mammals and birds. The invention also provides for an improved method for eradicating, controlling and preventing parasite infestation in birds and mammals.
    本发明提供了公式(I)的环状脱肽化合物,其中至少一个碳原子的立体化学构型与自然存在的环状脱肽PF1022A的基团Cy1、Cy2、R1、R2、R3、R4、Ra和Rb相比发生了倒置。该发明还提供了包含这些化合物的组合物,对危害动物的寄生虫具有有效性。这些化合物和组合物可用于对抗哺乳动物和鸟类体内或体表的寄生虫。该发明还提供了一种改进的方法,用于根除、控制和预防鸟类和哺乳动物的寄生虫感染。
  • FUSED BICYCLIC HETEROCYCLE DERIVATIVES AS PESTICIDES
    申请人:Bayer Aktiengesellschaft
    公开号:US20200383334A1
    公开(公告)日:2020-12-10
    The invention relates to novel compounds of the formula (I) in which Aa, Ab, Ac, Ad, Q, R 1 and n have the definitions given above, to their use as acaricides and/or insecticides for controlling animal pests and to processes and intermediates for their preparation.
    这项发明涉及公式(I)的新化合物, 其中Aa、Ab、Ac、Ad、Q、R1和n具有上述给定的定义, 以及它们作为杀螨剂和/或杀虫剂用于控制动物害虫的用途,以及用于它们制备的工艺和中间体。
  • [EN] ANTI PARASITIC DIHYDROAZOLE COMPOUNDS AND COMPOSITIONS COMPRISING SAME<br/>[FR] DIHYDROAZOLES ANTIPARASITAIRES ET COMPOSITIONS LES INCLUANT
    申请人:MERIAL LTD
    公开号:WO2011075591A1
    公开(公告)日:2011-06-23
    The present invention relates to novel dihydroazole of formula (I) and salts thereof: Wherein R1, A1, A2, G, X and Y are as defined in the description, compositions thereof, processes for their preparation and their uses to prevent or treat parasitic infections or infestations in animals and as pesticides.
    本发明涉及式(I)的新型二氢咪唑及其盐:其中R1、A1、A2、G、X和Y如描述中所定义,以及它们的组合物、制备方法以及它们用于预防或治疗动物寄生虫感染或寄生虫侵袭以及作为杀虫剂的用途。
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