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1-[(6-chloro-3-pyridinyl)-methyl]pyridine-2(1H)-imine

中文名称
——
中文别名
——
英文名称
1-[(6-chloro-3-pyridinyl)-methyl]pyridine-2(1H)-imine
英文别名
1-((6-chloropyridin-3-yl)methyl)pyridine-2(1H)-imine;1-[(6-chloropyridin-3-yl)methyl]pyridine-2(1H)-imine;1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine;1-[(6-Chloropyridin-3-yl)methyl]pyridin-2-imine
1-[(6-chloro-3-pyridinyl)-methyl]pyridine-2(1H)-imine化学式
CAS
——
化学式
C11H10ClN3
mdl
——
分子量
219.673
InChiKey
DSSGEOZAQMMSSU-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):
    1.9
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    40
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

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文献信息

  • PEST CONTROL AGENT
    申请人:KAGABU Shinzo
    公开号:US20130150414A1
    公开(公告)日:2013-06-13
    Specific amine derivatives have been found to possess excellent activities as pest control agents.
    特定的胺衍生物被发现具有优秀的杀虫剂活性。
  • [EN] N-SUBSTITUTED IMINO HETEROCYCLIC COMPOUNDS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES DE TYPE IMINO N-SUBSTITUÉS
    申请人:BASF SE
    公开号:WO2015091649A1
    公开(公告)日:2015-06-25
    The present invention relates to N-substituted imino compound of formula (I), wherein Y is a radical Y1, Y2, Y3, Y4 or Y5, where Y1 is O-C(=X)-R3; Y2 is S-C(=X)-R3; Y3 is N(R5)-C(=X)-R3; Y4 is N(R5)-S(=O)-R4; Y5 is N(R5)-S(=O)2-R4; and where X is O or S; Het is a 5 or 6 membered carbon-bound or nitrogen-bound heterocyclic ring, W1-W2-W3-W4 represents a carbon chain group connected to N and C=N, and thus forming a saturated, unsaturated, or partially unsaturated 5 or 6 membered nitrogen containing heterocycle, wherein W1, W2, W3 and W4 each individually represent CRVRW; R1, R2 may be hydrogen, halogen, C1-C6-alkyl etc.; and where R3, R4 and R5 are as defined herein. The invention also relates to the use of the N-acylimino heterocyclic compounds, their stereoisomers, their tautomers and their salts, for combating invertebrate pests. Furthermore the invention relates also to methods of combating invertebrate pests, which comprises applying such compounds.
    本发明涉及式(I)的N-取代亚胺化合物,其中Y是基团Y1、Y2、Y3、Y4或Y5,其中Y1为O-C(=X)-R3;Y2为S-C(=X)-R3;Y3为N(R5)-C(=X)-R3;Y4为N(R5)-S(=O)-R4;Y5为N(R5)-S(=O)2-R4;其中X为O或S;Het为5或6成员碳键或氮键杂环环,W1-W2-W3-W4代表连接至N和C=N的碳链基团,从而形成饱和、不饱和或部分不饱和的含氮5或6成员杂环,其中W1、W2、W3和W4各自表示CRVRW;R1、R2可以是氢、卤素、C1-C6-烷基等;R3、R4和R5如本文所定义。本发明还涉及N-酰基亚胺杂环化合物及其立体异构体、互变异构体和盐的用途,用于对抗无脊椎动物害虫。此外,本发明还涉及用于对抗无脊椎动物害虫的方法,包括应用这些化合物。
  • Heterocyclic compounds having effect of activating a4beta2 nicotinic acetylcholine receptors
    申请人:SUNTORY LIMITED
    公开号:US20020028809A1
    公开(公告)日:2002-03-07
    There is provided heterocyclic compounds of the following formula (I): 1 in which, A is optionally substituted aryl group or optionally substituted heterocyclic group; X is oxygen atom, sulfur atom, carbon atom or nitrogen atom; dotted line shows either presence or absence of bond; n is integer of 1 or 2; and Y represents alkylene bond and so on; or a pharmaceutically acceptable salt thereof. These compounds have good affinity to &agr;4&bgr;2 nicotinic acetylcholine receptors and activate the same to thereby exert a preventive or therapeutic effect on cerebral dysfunction.
    提供了以下式子(I)的杂环化合物:1其中,A是可选择取代的芳基或可选择取代的杂环基;X是氧原子、硫原子、碳原子或氮原子;虚线表示键的存在或不存在;n是1或2的整数;Y表示烷基键等;或其药学上可接受的盐。这些化合物与α4β2型尼古丁乙酰胆碱受体具有良好的亲和力,并激活它们,从而对脑功能障碍产生预防或治疗作用。
  • Flupyrimin: A Novel Insecticide Acting at the Nicotinic Acetylcholine Receptors
    作者:Yasumichi Onozaki、Ryo Horikoshi、Ikuya Ohno、Shigeki Kitsuda、Kathleen A. Durkin、Tomonori Suzuki、Chiaki Asahara、Natsuko Hiroki、Rena Komabashiri、Rikako Shimizu、Shogo Furutani、Makoto Ihara、Kazuhiko Matsuda、Masaaki Mitomi、Shinzo Kagabu、Katsuhito Uomoto、Motohiro Tomizawa
    DOI:10.1021/acs.jafc.7b02924
    日期:2017.9.13
    A novel chemotype insecticide flupyrimin (FLP) [N-[(E)-1-(6-chloro-3-pyridinylmethyl)pyridin-2(1H)-ylidene]-2,2,2-trifluoroacetamide], discovered by Meiji Seika Pharma, has unique biological properties, including outstanding potency to imidacloprid (IMI)-resistant rice pests together with superior safety toward pollinators. Intriguingly, FLP acts as a nicotinic antagonist in American cockroach neurons
    明治大学发现了​​一种新型化学型杀虫剂氟嘧啶(FLP)[ N -[(E)-1-(6-氯-3-吡啶基甲基)吡啶-2-2(1 H)-亚烷基] -2,2,2-三氟乙酰胺] Seika Pharma具有独特的生物学特性,包括对耐吡虫啉(IMI)的水稻害虫具有出色的效力,以及对传粉媒介的优越安全性。有趣的是,FLP在美国蟑螂神经元中充当烟碱拮抗剂,[ 3 H] FLP与家蝇烟碱乙酰胆碱(ACh)受体(nAChR)制剂中的多个高亲和力结合成分结合。[ 3H] FLP受体与IMI受体相同,替代方案是对IMI不敏感的亚型。此外,如对大鼠α4β2nAChR的亲和力极低所预测的那样,FLP对大鼠安全有利。FLP类似物在受体效能方面的结构-活性关系得到了检验,其特征在于吡啶基亚吡啶和三氟乙酰基药效基团,从而建立了在加州ApACh结合蛋白(昆虫nAChR的合适结构替代物)上的FLP分子识别。这些FLP药效基团具有
  • NITROGEN-CONTAINING HETEROCYCLIC DERIVATIVE HAVING 2-IMINO GROUP AND PEST CONTROL AGENT INCLUDING THE SAME
    申请人:MEIJI SEIKA PHARMA CO., LTD.
    公开号:US20150005347A1
    公开(公告)日:2015-01-01
    Provided is a nitrogen-containing heterocyclic derivative having a 2-imino group, which is represented by the following Formula (I). [in the formula, Ar represents a phenyl group which may be substituted, a 5- to 6-membered heterocycle which may be substituted, or a 4- to 10-membered heterocycloalkyl group, A represents a heterocycle having a 5- to 10-membered unsaturated bond including one or more nitrogen atoms, and has an imino group substituted with an R group at a position adjacent to the nitrogen atom present on the cycle, Y represents a hydrogen atom, a halogen atom, a hydroxyl group, a C1 to C6 alkyl group which may be substituted with a halogen atom, a C1 to C6 alkyloxy group which may be substituted with a halogen atom, a cyano group, or a nitro group, and R represents any one of groups represented by the following Formulae (a) to (e), (y) or (z).]
    提供的是一种含氮杂环衍生物,具有2-亚氨基基团,其化学式如下(I)所示。[在该式中,Ar代表可能被取代的苯基,可能被取代的5-至6-元杂环或4-至10-元杂环烷基基团,A代表含有5-至10-元不饱和键的杂环,其中包括一个或多个氮原子,并且在环上存在一个邻位于氮原子处的被R基取代的亚氨基,Y代表氢原子、卤素原子、羟基、可能被卤素原子取代的C1至C6烷基、可能被卤素原子取代的C1至C6烷氧基、氰基或硝基,R代表以下化学式(a)至(e)、(y)或(z)中的任意一种基团。]
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