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Nitrogen hydrogen | 152204-31-4

中文名称
——
中文别名
——
英文名称
Nitrogen hydrogen
英文别名
molecular hydrogen;molecular nitrogen
Nitrogen hydrogen化学式
CAS
152204-31-4
化学式
H2*N2
mdl
——
分子量
30.0293
InChiKey
ZYXVCTMQFLMBPQ-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):
    0.28
  • 重原子数:
    2
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    47.6
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    Nitrogen hydrogen 反应 4.0h, 生成
    参考文献:
    名称:
    通过引入钛增强了二氧化铈负载的Ru催化剂的氨合成性能。
    摘要:
    Ti物种的空间排列将影响二氧化铈负载的Ru催化剂的电子-金属相互作用和Ce3 +位点的比例。Ti表面负载的CeO2负载Ru催化剂表现出优异的氨合成活性,这归因于Ru金属的比例更大,Ru物种的电子更多以及氢和氮的吸附能力更好。
    DOI:
    10.1039/c9cc07385j
  • 作为试剂:
    描述:
    、 5-bromo-N-[(4,6-dimethyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]-1-methyl-3-(1-methylethyl)-1H-indole-7-carboxamide 、 三乙胺Nitrogen hydrogen乙醇氢气methanol-dichloromethane二氯甲烷 、 silica gel 、 silica 作用下, 以 乙醇四氢呋喃二氯甲烷氯仿 为溶剂, 反应 20.25h, 生成 ammonia methanol 、 N-[(4,6-dimethyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]-1-methyl-3-(1-methylethyl)-1H-indole-7-carboxamide
    参考文献:
    名称:
    INDOLES
    摘要:
    本文披露了公式(I)中各个基团的吲哚类化合物,这些化合物对治疗癌症有用。
    公开号:
    US20130245016A1
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文献信息

  • Combinations of Pyrazole Kinase Inhibitors and Further Antitumor Agents
    申请人:Curry Jayne Elizabeth
    公开号:US20080161355A1
    公开(公告)日:2008-07-03
    The invention provides a combination of a compound having the formula (0) and two or more further anti-cancer agents: or salts or tautomers or N-oxides or solvates thereof; wherein X is a group R 1 -A-NR 4 — or a 5- or 6-membered carbocyclic or heterocyclic ring; A is a bond, SO2, C═O, NR 9 (C═O) or 0(C═O) wherein R 9 is hydrogen or C 1-4 hydrocarbyl optionally substituted by hydroxy or C 1-4 alkoxy; Y is a bond or an alkylene chain of 1, 2 or 3 carbon atoms in length; R 1 is hydrogen; a carbocyclic or heterocyclic group having from 3 to 12 ring members; or a C 1-8 hydrocarbyl group optionally substituted by one or more substituents selected from halogen (e.g. fluorine), hydroxy, C 1-4 hydrocarbyloxy, amino, mono- or di-C 1-4 hydrocarbylamino, and carbocyclic or heterocyclic groups having from 3 to 12 ring members, and wherein 1 or 2 of the carbon atoms of the hydrocarbyl group may optionally be replaced by an atom or group selected from O, S, NH, SO, SO 2 ; R 2 is hydrogen; halogen; C 1-4 alkoxy (e.g. methoxy); or a C 1-4 hydrocarbyl group optionally substituted by halogen (e.g. fluorine), hydroxyl or C 1-4 alkoxy (e.g. methoxy); R 3 is selected from hydrogen and carbocyclic and heterocyclic groups having from 3 to 12 ring members; and R 4 is hydrogen or a C 1-4 hydrocarbyl group optionally substituted by halogen (e.g. fluorine), hydroxyl or C 1-4 alkoxy (e.g. methoxy).
    本发明提供了一种由具有公式(0)的化合物和两种或更多进一步的抗癌剂组成的组合物:或其盐或互变异构体或N-氧化物或溶剂化物;其中X是一个R1-A-NR4-或一个5-或6-成员的碳环或杂环环;A是一个键,SO2,C═O,NR9(C═O)或0(C═O),其中R9是氢或C1-4烃基,可以选择地被羟基或C1-4烷氧基取代;Y是一个键或长度为1、2或3个碳原子的烷基链;R1是氢;具有3到12个环成员的碳环或杂环基团;或者是一个C1-8烃基,可以选择地被一个或多个取代基所取代,所述取代基选自卤素(例如)、羟基、C1-4烃氧基、基、单-或双C1-4烃基基和具有从3到12个环成员的碳环或杂环基团,其中烃基的1或2个碳原子可以选择性地被O、S、NH、SO、SO2中的一个原子或基取代;R2是氢;卤素;C1-4烷氧基(例如甲氧基);或一个C1-4烃基,可以选择地被卤素(例如)、羟基或C1-4烷氧基(例如甲氧基)所取代;R3选自氢和具有从3到12个环成员的碳环和杂环基团;R4是氢或一个C1-4烃基,可以选择地被卤素(例如)、羟基或C1-4烷氧基(例如甲氧基)所取代。
  • Pharmaceutical Compounds
    申请人:Curry Jayne Elizabeth
    公开号:US20080161251A1
    公开(公告)日:2008-07-03
    The invention provides a combination of a cytotoxic compound or signalling inhibitor and a compound having the formula (0): or salts or tautomers or N-oxides or solvates thereof; wherein X is a group R 1 -A-NR 4 - or a 5- or 6-membered carbocyclic or heterocyclic ring; A is a bond, SO 2 , C═O, NR g (C═O) or 0(C═O) wherein R g is hydrogen or C 1-4 hydrocarbyl optionally substituted by hydroxy or C 1-4 alkoxy; Y is a bond or an alkylene chain of 1, 2 or 3 carbon atoms in length; R 1 is hydrogen; a carbocyclic or heterocyclic group having from 3 to 12 ring members; or a C 1-8 hydrocarbyl group optionally substituted by one or more substituents selected from halogen (e.g. fluorine), hydroxy, C 1-4 hydrocarbyloxy, amino, mono- or di-C 1-4 hydrocarbylamino, and carbocyclic or heterocyclic groups having from 3 to 12 ring members, and wherein 1 or 2 of the carbon atoms of the hydrocarbyl group may optionally be replaced by an atom or group selected from O, S, NH, SO, SO 2 ; R 2 is hydrogen; halogen; C 1-4 alkoxy (e.g. methoxy); or a C 1-4 hydrocarbyl group optionally substituted by halogen (e.g. fluorine), hydroxyl or C 1-4 alkoxy (e.g. methoxy); R 3 is selected from hydrogen and carbocyclic and heterocyclic groups having from 3 to 12 ring members; and R 4 is hydrogen or a C 1-4 hydrocarbyl group optionally substituted by halogen (e.g. fluorine), hydroxyl or C 1-4 alkoxy (e.g. methoxy).
    本发明提供了一种细胞毒性化合物或信号抑制剂与式(0)的化合物或其盐、互变异构体、N-氧化物或溶剂化物的组合物;其中X是一个R1-A-NR4-或5-或6-成员的碳环或杂环;A是一个键,SO2,C═O,NRg(C═O)或0(C═O),其中Rg是氢或C1-4羟基或C1-4烷氧基取代的烷基;Y是一个键或1、2或3个碳原子长的烷基链;R1是氢;一个从3到12个环成员的碳环或杂环基团;或一个C1-8烷基基团,可选地取代一个或多个取代基,所述取代基选自卤素(例如)、羟基、C1-4烷氧基、基、C1-4单取代或双取代烷基基和从3到12个环成员的碳环或杂环基团,其中烷基基团的1或2个碳原子可以选为O、S、NH、SO或SO2中的原子或基团;R2是氢;卤素;C1-4烷氧基(例如甲氧基);或一个C1-4烷基基团,可选地取代卤素(例如)、羟基或C1-4烷氧基(例如甲氧基);R3选自氢和从3到12个环成员的碳环或杂环基团;R4是氢或一个C1-4烷基基团,可选地取代卤素(例如)、羟基或C1-4烷氧基(例如甲氧基)。
  • Process for the preparation of 2,6-dialkyl-N-alkylanilines
    申请人:Ciba-Geigy Corporation
    公开号:US04183868A1
    公开(公告)日:1980-01-15
    A process for the preparation of 2,6-dialkyl-N-alkylanilines is disclosed, which process comprises the reaction of a 2,6-dialkylaniline with an alkanol at 200.degree. to 350.degree. C. in the presence of a copper-containing catalyst which contains 0.05 to 10% by weight of palladium or platinum.
    公开了一种制备2,6-二烷基-N-烷基苯胺的方法,该方法包括在存在含有0.05至10重量%催化剂的情况下,在200℃至350℃下,将2,6-二烷基苯胺与烷醇反应。
  • Preparation of 2-alkylpyrimidines
    申请人:The Dow Chemical Company
    公开号:US04493929A1
    公开(公告)日:1985-01-15
    2-Alkylpyrimidines are obtained in a one step reaction which comprises the dehydrogenation of a 2-alkyltetrahydropyrimidine over a supported noble metal catalyst under conditions which do not generate water and in which no water is added.
    2-烷基嘧啶可以通过一步反应得到,该反应包括在不产生和不添加的条件下,在贵金属催化剂的支持下对2-烷基四氢嘧啶进行脱氢。
  • Plasma display unit
    申请人:——
    公开号:US20040239247A1
    公开(公告)日:2004-12-02
    A plasma display device includes a blue phosphor composed of a compound represented by Me 3 MgSi 2 O 8 :Eu (where, Me is at least calcium (Ca), strontium (Sr), or barium (Ba)). Concentration of bivalent Eu ions is 45 to 95% and concentration of trivalent Eu ions is 5 to 55%, of the europium (Eu) atoms contained in the blue phosphor layer. The plasma display device has less luminance degradation in a panel manufacturing process, high luminance, and long lifetime.
    一种等离子体显示器件包括由Me3MgSi2O8:Eu化合物组成的蓝色荧光体(其中,Me至少为(Ca)、(Sr)或(Ba))。二价Eu离子的浓度为45%至95%,三价Eu离子的浓度为5%至55%,其中包含在蓝色荧光体层中的Eu原子。该等离子体显示器件在面板制造过程中具有较少的亮度退化,高亮度和长寿命。
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