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(4,5-dihydro-oxazol-2-yl)-pentyl-amine | 90152-23-1

中文名称
——
中文别名
——
英文名称
(4,5-dihydro-oxazol-2-yl)-pentyl-amine
英文别名
N-pentyl-4,5-dihydro-1,3-oxazol-2-amine
(4,5-dihydro-oxazol-2-yl)-pentyl-amine化学式
CAS
90152-23-1
化学式
C8H16N2O
mdl
——
分子量
156.228
InChiKey
BXFVPHZJYSKQOY-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):
    1.4
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    33.6
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • N-ARYLAMIDINE-SUBSTITUTED TRIFLUOROETHYL SULFIDE DERIVATIVES AS ACARICIDES AND INSECTICIDES
    申请人:BAYER CROPSCIENCE AG
    公开号:US20140315898A1
    公开(公告)日:2014-10-23
    The present invention relates to novel N-arylamide-substituted trifluoroethyl sulfide derivatives of the formula (I) in which X 1 , X 2 , X 3 , X 4 , R 1 , R 2 , R 3 , n have the meanings given in the description—to their use as acaricides and insecticides for controlling animal pests and to processes and intermediates for their preparation
    本发明涉及公式(I)中的新型N-芳酰胺取代三乙基醚衍生物,其中X1、X2、X3、X4、R1、R2、R3、n的含义如描述所示—它们作为杀螨剂杀虫剂用于控制动物害虫,并涉及其制备的过程和中间体。
  • [EN] 1,3-HETEROCYCLES CONDENSED WITH MONOTERPENE SKELETON, THEIR USE AND PHARMACEUTICAL COMPOSITIONS COMPRISING SUCH COMPOUNDS<br/>[FR] HÉTÉROCYCLES-1,3 CONDENSÉS AVEC UN SQUELETTE MONOTERPÉNIQUE, UTILISATION DE CEUX-CI ET COMPOSITIONS PHARMACEUTIQUES COMPRENANT DE TELS COMPOSÉS
    申请人:BIOBLOCKS MAGYARORSZAG GYOGYSZ
    公开号:WO2010070365A1
    公开(公告)日:2010-06-24
    The invention relates to chiral compounds with monoterpene skeleton of general formula (I) - where in the formula X stands for O or H2; W stands for O, S, N-R2 or Ph-R3; Y stands for O or N-R4; R1 stands for H, C1-4Alk or (C2)1-4-Ph; R2 stands for C1-4Alk or Ph-R3; R3 stands for H, C1-4Alk, C1-4Alk-O or Hlg; R4 stands for H or Ph; and one of the signs --- means the presence of a double bond and the other means the absense of a double bond, with the proviso that only one of W and Y may simultaneously stand for oxygen - as well as to their prodrugs and salts formed with pharmaceutically acceptable acids. Furthermore, the invention relates to cytostatic pharmaceutical compositions comprising one or more compounds of general formula (I) and usual inert pharmaceutical carriers and/or auxiliary agents, to the use of the compounds of general formula (I) for preparing cytostatic pharmaceutical compositions as well as to the treatment and/or curing of cancerous illnesses.
    本发明涉及具有单萜骨架的手性化合物,其通式为(I)-其中在式中,X代表O或H2; W代表O、S、N-R2或Ph-R3; Y代表O或N-R4; R1代表H、C1-4Alk或(C2)1-4-Ph; R2代表C1-4Alk或Ph-R3; R3代表H、C1-4Alk、C1-4Alk-O或Hlg; R4代表H或Ph; 而---符号之一表示存在双键,另一个表示不存在双键,但W和Y中只有一个可以同时代表氧-以及它们的前药和与药学上可接受的酸形成的盐。此外,本发明还涉及包含一种或多种通式(I)化合物和通常的惰性药物载体和/或辅助剂的细胞毒药物组合物,以及使用通式(I)化合物制备细胞毒药物组合物以及治疗和/或治愈癌症疾病的方法。
  • Substituted 2-arylimino heterocycles and compositions containing them for use as progesterone receptor binding agents
    申请人:——
    公开号:US20030207865A1
    公开(公告)日:2003-11-06
    This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.
    本发明涉及2-芳基亚胺杂环,包括2-芳基亚胺-1,3-噻唑啉,2-芳基亚胺-2,3,4,5-四氢-1,3-噻嗪,2-芳基亚胺-1,3-噻唑啉-4-酮,2-芳基亚胺-1,3-噻唑啉-5-酮和2-芳基亚胺-1,3-噁唑啉,以及它们在调节孕激素受体介导的过程中的应用,以及用于这种治疗的制药组合物。
  • Indanyl- and Tetrahydronaphthyl-Amino-Azoline Compounds for Combating Animal Pests
    申请人:Kordes Markus
    公开号:US20080293569A1
    公开(公告)日:2008-11-27
    The present invention relates to Indanyl- and Tetrahydronaphthyl-amino-azoline compounds of formula I wherein the variables R 1 and R 2 are as defined in description. The invention relates also to methods of combating or controlling insects, arachnids or nematodes, to methods for protecting growing plants from attack or infestation by insects, arachnids or nematodes, to methods for the protection of seeds from soil insects and of the seedlings' roots and shoots from soil and foliar insects and to methods for treating, controlling, preventing or protecting animals against infestation or infection by parasites.
    本发明涉及公式I的Indanyl和Tetrahydronaphthyl-amino-azoline化合物,其中变量R1和R2如描述中所定义。本发明还涉及用于对抗或控制昆虫、蜘蛛或线虫的方法,用于保护生长中的植物免受昆虫、蜘蛛或线虫的攻击或侵染的方法,用于保护种子免受土壤昆虫和幼苗的根和茎免受土壤和叶面昆虫的侵染的方法,以及用于治疗、控制、预防或保护动物免受寄生虫感染或侵染的方法。
  • Insecticidal Substituted Amino Heterocyclic and Heteroaryl Derivatives
    申请人:Dixon John A.
    公开号:US20100137385A1
    公开(公告)日:2010-06-03
    Certain substituted amino heterocyclic and heteroaryl derivatives have provided unexpected insecticidal and acaricidal activity. These compounds are represented by formula (I): wherein R, R 1 , R 2 , R 3 , R 4 , A, B and Q are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I, and optionally, an effective amount of at least one of an additional compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present.
    某些取代基杂环和杂环基衍生物表现出意外的杀虫和杀螨活性。这些化合物由公式(I)表示:其中R,R1,R2,R3,R4,A,B和Q在此完全描述。此外,还公开了包含公式I中至少一种化合物的杀虫有效量和可选地至少一种额外化合物的有效量,并带有至少一种杀虫兼容载体的组合物;以及通过将上述组合物应用于存在或预计存在昆虫的地点来控制昆虫的方法。
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