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2-氯-6-甲基-4-嘧啶甲腈 | 16858-56-3

中文名称
2-氯-6-甲基-4-嘧啶甲腈
中文别名
2-氯-6-甲基-4-腈基嘧啶
英文名称
2-chloro-6-methylpyrimidine-4-carbonitrile
英文别名
——
2-氯-6-甲基-4-嘧啶甲腈化学式
CAS
16858-56-3
化学式
C6H4ClN3
mdl
MFCD09878518
分子量
153.571
InChiKey
SDYFYBAYSDNFRP-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:
    45-46 °C(Solv: ligroine (8032-32-4))
  • 沸点:
    324.5±22.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    49.6
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2933599090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302+H312+H332,H315,H319,H335

SDS

SDS:2b1c28c64181637939536bb4025f260a
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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

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文献信息

  • [EN] BRIDGED DIAZEPANE OREXIN RECEPTOR ANTAGONISTS<br/>[FR] COMPOSÉS DE DIAZÉPANE PONTÉS UTILES EN TANT QU'ANTAGONISTES DES RÉCEPTEURS D'OREXINE
    申请人:MERCK SHARP & DOHME
    公开号:WO2016085783A1
    公开(公告)日:2016-06-02
    The present invention is directed to bridged diazepane compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.
    本发明涉及桥联二氮杂环庚烷化合物,其为俄雷欣受体拮抗剂。本发明还涉及所述化合物在潜在的治疗或预防涉及俄雷欣受体的神经和精神障碍和疾病中的用途。本发明还涉及包含这些化合物的组合物。本发明还涉及这些组合物在潜在的预防或治疗涉及俄雷欣受体的疾病中的用途。
  • [EN] INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION<br/>[FR] INHIBITEURS DE LA RÉPLICATION DU VIRUS DE L'IMMUNODÉFICIENCE HUMAINE
    申请人:VIIV HEALTHCARE UK NO 5 LTD
    公开号:WO2021064677A1
    公开(公告)日:2021-04-08
    Compounds of Formula I, including pharmaceutically acceptable salts thereof, and compositions and methods for treating human immunodeficiency virus (HIV) infection are set forth: Formula I.
    公式I的化合物,包括其药用可接受的盐,以及用于治疗人类免疫缺陷病毒(HIV)感染的组合物和方法如下:公式I。
  • Heterocyclic Compound
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20180155333A1
    公开(公告)日:2018-06-07
    The present invention provide a compound having an orexin receptor antagonistic activity, which is expected to be useful as medicaments such as agents for the prophylaxis or treatment of sleep disorder, depression, anxiety disorder, panic disorder, schizophrenia, drug dependence, Alzheimer's disease and the like. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.
    本发明提供了一种具有促醒素受体拮抗活性的化合物,预计可用作药物,如预防或治疗睡眠障碍、抑郁症、焦虑症、恐慌症、精神分裂症、药物依赖、阿尔茨海默病等的药剂。 本发明涉及由以下式(I)表示的化合物: 其中每个符号如规范中定义,或其盐。
  • [EN] NOVEL PYRIMIDINE-PYRIDINE DERIVATIVES<br/>[FR] NOUVEAUX DÉRIVÉS DE PYRIMIDINE-PYRIDINE
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2009109907A1
    公开(公告)日:2009-09-11
    The invention relates to novel pyrimidine-pyridine derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunomodulating agents. Formula I.
    本发明涉及新颖的嘧啶-吡啶衍生物、其制备方法及其作为药理活性化合物的应用。所述化合物特别作为免疫调节剂发挥作用。式I。
  • Herbicidal compounds
    申请人:American Cyanamid Company
    公开号:US05759956A1
    公开(公告)日:1998-06-02
    A compound of the general formula (I) ##STR1## wherein A represents a group of general formula ##STR2## and R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, X, Q.sup.2, Q.sup.3, and n are as described in the specification. The compounds of formula (I) are useful as agricultural herbicides.
    一种通式(I)的化合物,其中A代表通式(II)的一种基团##STR2## R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、R.sup.6、X、Q.sup.2、Q.sup.3和n的含义如说明书所述。式(I)的化合物可作为农业除草剂使用。
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