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3-苄基腺嘌呤 | 103984-25-4

中文名称
3-苄基腺嘌呤
中文别名
——
英文名称
3-benzyladenine
英文别名
2-benzyl-7(9)H-purin-6-ylamine;US9138393, 3-Benzyladenine;2-benzyl-7H-purin-6-amine
3-苄基腺嘌呤化学式
CAS
103984-25-4
化学式
C12H11N5
mdl
——
分子量
225.253
InChiKey
LHPVTMAMEMZFIJ-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

  • 沸点:
    377.3±52.0 °C(Predicted)
  • 密度:
    1.44±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    80.5
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    甲酸 、 2-Benzyl-4,6-diamino-5-nitroso-pyrimidin 在 sodium dithionite 、 formamide 作用下, 生成 3-苄基腺嘌呤
    参考文献:
    名称:
    Synthesis of 2-Aminonicotinamides by Raney Nickel Cleavage of Pyrazolo[3,4-b]-pyridines1
    摘要:
    DOI:
    10.1021/ja01519a043
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文献信息

  • [EN] PYRIDINE COMPOUND, PESTICIDAL COMPOSITION AND METHOD OF CONTROLLING PEST<br/>[FR] COMPOSÉ DE PYRIDINE, COMPOSITION PESTICIDE ET PROCÉDÉ DE LUTTE CONTRE LES NUISIBLES
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2009066786A1
    公开(公告)日:2009-05-28
    A pyridine compound represented by the following general formula (1); the pyridine compound in which R1 is a C1-C3 fluoroalkyl group or a C1-C3 fluoroalkoxy group; the pyridine compound in which R2 is a hydrogen atom; the pyridine compound in which R2 is a group represented by Q1; a pesticidal composition containing the pyridine compound as an active ingredient; and a method of controlling a pest including applying an effective amount of the pyridine compound to the pest or a place where the pest inhabits, are provided.
    以下是通用公式(1)表示的吡啶化合物;其中R1是C1-C3氟烷基或C1-C3氟烷氧基的吡啶化合物;其中R2是氢原子的吡啶化合物;其中R2是由Q1表示的基团的吡啶化合物;包含所述吡啶化合物作为活性成分的杀虫剂组合物;以及一种控制害虫的方法,包括向害虫或害虫栖息地施加有效量的吡啶化合物。
  • HETEROARYLAZOLE COMPOUND AND PEST CONTROL AGENT
    申请人:Nippon Soda Co., Ltd.
    公开号:US20210380556A1
    公开(公告)日:2021-12-09
    An object of the present invention is to provide a heteroaryl azole compound that is excellent in pest control activity, particularly, insecticidal activity and/or miticidal activity, is excellent in safety, and may be industrially advantageously synthesized. The compound of the present invention is a compound represented by the formula (I), an N-oxide compound, stereoisomer, tautomer or hydrate thereof or a salt of any of these compounds. In the formula (I), A represents CH or a nitrogen atom; B 1 represents CX 1 or a nitrogen atom; X 1 , X 2 and X 3 each independently represent a hydrogen atom, a substituted or unsubstituted C1-6 alkyl group, a substituted or unsubstituted C2-6 alkenyl group, or the like; R 1 represents a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, or the like; R 2 represents a substituted or unsubstituted C1-6 alkyl group; and R represents a substituted or unsubstituted C1-6 alkyl group.
    本发明的一个目的是提供一种在害虫控制活性方面表现出色,特别是在杀虫活性和/或杀螨活性方面表现出色,安全性优秀,并且可以在工业上有利地合成的杂环芳醇类化合物。本发明的化合物是由式(I)表示的化合物,其N-氧化物化合物,立体异构体,互变异构体或其水合物,或这些化合物的任何盐。在式(I)中,A代表CH或氮原子;B1代表CX1或氮原子;X1,X2和X3分别独立地代表氢原子,取代或未取代的C1-6烷基基团,取代或未取代的C2-6烯基基团,或类似物;R1代表取代或未取代的C1-6烷基硫基团,取代或未取代的C1-6烷基亚硫氧基团,或类似物;R2代表取代或未取代的C1-6烷基基团;R代表取代或未取代的C1-6烷基基团。
  • (HETERO)ARYLIMIDAZOLE COMPOUND AND HARMFUL ORGANISM CONTROL AGENT
    申请人:Nippon Soda Co., Ltd.
    公开号:US20210380554A1
    公开(公告)日:2021-12-09
    An object of the present invention is to provide a (hetero)aryl imidazole compound that is excellent in pest control activity, particularly, insecticidal activity and/or acaricidal activity, is excellent in safety, and may be industrially advantageously synthesized. The (hetero)aryl imidazole compound of the present invention is a compound represented by the formula (I) an N-oxide compound, stereoisomer, tautomer or hydrate thereof or a salt of any of these compounds. In the formula (I), B 1 represents a nitrogen atom or CH; X represents a substituted or unsubstituted C3-8 cycloalkyl group; R 1 represents a substituted or unsubstituted C1-6 alkylthio group or a substituted or unsubstituted C1-6 alkylsulfonyl group; R 2 represents a substituted or unsubstituted C1-6 alkyl group; and R represents a substituted or unsubstituted C2-6 alkenyl group.
    本发明的一个目的是提供一种在害虫控制活性方面表现出色,特别是在杀虫活性和/或杀螨活性方面表现出色,安全性优秀,并且可以在工业上有利地合成的(杂)芳基咪唑化合物。本发明的(杂)芳基咪唑化合物是由以下式(I)表示的化合物 一种N-氧化物化合物,立体异构体,互变异构体或其水合物,或这些化合物的任何盐。在式(I)中,B 1 代表氮原子或CH;X代表取代或未取代的C3-8环烷基基团;R 1 代表取代或未取代的C1-6烷硫基团或取代或未取代的C1-6烷基磺酰基团;R 2 代表取代或未取代的C1-6烷基基团;而R代表取代或未取代的C2-6烯基基团。
  • Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK)
    申请人:CHEN Han-Min
    公开号:US20140303112A1
    公开(公告)日:2014-10-09
    The present invention relates to a method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) and the use of the compounds in the prevention or treatment of disease, including pre-diabetes, type 2 diabetes, syndrome X, metabolic syndrome and obesity.
    本发明涉及一种治疗疾病或病情的方法,该疾病或病情容易通过AMPK激活剂和公式化合物得到改善,这些化合物有助于激活AMP激活蛋白激酶(AMPK),并将这些化合物用于预防或治疗疾病,包括糖尿病前期、2型糖尿病、X综合症、代谢综合征和肥胖症。
  • DIARYL-AZOLE COMPOUND AND FORMULATION FOR CONTROLLING HARMFUL ORGANISM
    申请人:Nippon Soda Co., Ltd.
    公开号:US20190185459A1
    公开(公告)日:2019-06-20
    A compound represented by Formula (I), or a salt thereof: wherein, R 1 represents an unsubstituted or substituted C1-6 alkylthio group, or the like; A 1 represents a nitrogen atom or CH; A 2 represents a nitrogen atom or CR 2 ; R 2 and R 3 each independently represents a hydrogen atom, an unsubstituted or substituted C6-10 aryl group, an unsubstituted or substituted 3- to 6-membered heterocyclyl group, or the like; B 1 and B 2 each independently represents a nitrogen atom or CR 5 , with the proviso that B 1 and B 2 do not represent CR 5 at the same time, wherein R 5 represents a hydrogen atom, an unsubstituted or substituted C1-6 alkyl group, or the like; R 4 represents an unsubstituted or substituted C1-6 alkyl group, or the like, and R 4 binds to any one of nitrogen atoms forming an imidazole ring or a triazole ring; and Ar represents an unsubstituted or substituted C6-10 aryl group or the like.
    通过公式(I)表示的化合物,或其盐:其中,R1代表未取代或取代的C1-6烷基硫基团等;A1代表氮原子或CH;A2代表氮原子或CR2;R2和R3各自独立地代表氢原子、未取代或取代的C6-10芳基团、未取代或取代的3-至6-成员杂环基团等;B1和B2各自独立地代表氮原子或CR5,但须注意B1和B2不同时代表CR5,其中R5代表氢原子、未取代或取代的C1-6烷基团等;R4代表未取代或取代的C1-6烷基团等,且R4与形成咪唑环或三唑环的任一氮原子结合;Ar代表未取代或取代的C6-10芳基团等。
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