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1-sec-butyl-3-methylurea | 38014-55-0

中文名称
——
中文别名
——
英文名称
1-sec-butyl-3-methylurea
英文别名
1-sec-butyl-3-methylylurea;N-Methyl-N'-sec-butyl-harnstoff;N-Methyl-N'-s-butylharnstoff;N-Butan-2-yl-N'-methylurea;1-butan-2-yl-3-methylurea
1-sec-butyl-3-methylurea化学式
CAS
38014-55-0
化学式
C6H14N2O
mdl
MFCD00027886
分子量
130.19
InChiKey
RCRZYXFYHZOCJQ-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):
    0.7
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.833
  • 拓扑面积:
    41.1
  • 氢给体数:
    2
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2924199090

SDS

SDS:ee95800e6823b5708b870bce7c6d4202
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反应信息

  • 作为反应物:
    描述:
    1-sec-butyl-3-methylurea硫酸 、 sodium nitrite 作用下, 以 甲醇 为溶剂, 以63%的产率得到N-Methyl-N'-sec-butyl-N-nitrosourea
    参考文献:
    名称:
    Conformational preferences in alkylnitrosoureas
    摘要:
    DOI:
    10.1021/jo01293a023
  • 作为产物:
    描述:
    仲丁胺异氰酸甲酯乙醚 为溶剂, 以92%的产率得到1-sec-butyl-3-methylurea
    参考文献:
    名称:
    Conformational preferences in alkylnitrosoureas
    摘要:
    DOI:
    10.1021/jo01293a023
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文献信息

  • [EN] Aminotetraline derivatives, pharmaceutical compositions containing them, and their use in therapy<br/>[FR] DÉRIVÉS D'AMINOTÉTRALINE, COMPOSITIONS PHARMACEUTIQUES LES CONTENANT ET LEUR UTILISATION EN THÉRAPIE
    申请人:ABBOTT GMBH & CO KG
    公开号:WO2010092180A1
    公开(公告)日:2010-08-19
    The present invention relates to aminotetraline derivatives of the formula (I) or a physiologically tolerated salt thereof. The invention relates to pharmaceutical compositions comprising such aminotetraline derivatives, and the use of such aminotetraline derivatives for therapeutic purposes. The aminotetraline derivatives are GIyT1 inhibitors.
    本发明涉及式(I)的氨基四氢喹啉衍生物或其生理可容忍的盐。该发明涉及包含这样的氨基四氢喹啉衍生物的药物组合物,以及将这样的氨基四氢喹啉衍生物用于治疗目的。所述氨基四氢喹啉衍生物是GIyT1抑制剂。
  • PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS
    申请人:Philippe Michel
    公开号:US20100028280A1
    公开(公告)日:2010-02-04
    The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.
    该发明涉及一种直发角蛋白纤维的拉直过程,包括:(i)将至少两种变性剂含有的拉直组合物涂抹到角蛋白纤维上的步骤,(ii)使用加热装置将角蛋白纤维的温度升高至110至250°C的步骤。
  • AMINOINDANE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THEIR USE IN THERAPY
    申请人:POHLKI Frauke
    公开号:US20120040948A1
    公开(公告)日:2012-02-16
    The present invention relates to aminoindane derivatives of the formula (I) or a physiologically tolerated salt thereof. The invention relates to pharmaceutical compositions comprising such aminoindane derivatives, and the use of such aminoindane derivatives for therapeutic purposes. The aminoindane derivatives are GlyT1 inhibitors.
    本发明涉及公式(I)的氨基茚衍生物或其生理耐受的盐。该发明涉及包含这种氨基茚衍生物的药物组合物,以及利用这种氨基茚衍生物进行治疗的用途。这些氨基茚衍生物是GlyT1抑制剂。
  • N-SUBSTITUTED AMINOBENZOCYCLOHEPTENE, AMINOTETRALINE, AMINOINDANE AND PHENALKYLAMINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THEIR USE IN THERAPY
    申请人:AbbVie Deutschland GmbH & Co. KG
    公开号:US20130131132A1
    公开(公告)日:2013-05-23
    The present invention relates to N-substituted aminobenzocycloheptene, aminotetraline, aminoindane and phenalkylamine derivatives of the formula (I), (II), (III) or (IV) or a physiologically tolerated salt thereof. The invention relates to pharmaceutical compositions comprising such N-substituted aminobenzocycloheptene, aminotetraline, aminoindane and phenalkylamine derivatives, and the use of such N-substituted aminobenzocycloheptene, aminotetraline, aminoindane and phenalkylamine derivatives for therapeutic purposes. The N-substituted aminobenzocycloheptene, aminotetraline, aminoindane and phenalkylamine derivatives are GlyT1 inhibitors.
    本发明涉及式(I)、(II)、(III)或(IV)所示的N-取代氨基苯并环庚烯、氨基四氢异喹啉、氨基吲哚和苯基烷基胺衍生物 或其生理耐受盐。 该发明涉及包含上述N-取代氨基苯并环庚烯、氨基四氢异喹啉、氨基吲哚和苯基烷基胺衍生物的药物组合物,以及将上述N-取代氨基苯并环庚烯、氨基四氢异喹啉、氨基吲哚和苯基烷基胺衍生物用于治疗用途。所述N-取代氨基苯并环庚烯、氨基四氢异喹啉、氨基吲哚和苯基烷基胺衍生物是甘氨酸转运体1抑制剂。
  • [EN] BENZAZEPINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THEIR USE IN THERAPY<br/>[FR] DÉRIVÉS DE BENZAZÉPINE, COMPOSITIONS PHARMACEUTIQUES CONTENANT CEUX-CI, ET LEUR UTILISATION EN THÉRAPIE
    申请人:ABBOTT GMBH & CO KG
    公开号:WO2012152915A1
    公开(公告)日:2012-11-15
    The present invention relates to benzazepine derivatives of the formula (I) or a physiologically tolerated salt thereof. The present invention also relates to pharmaceutical compositions comprising such benzazepine derivatives, and the use of such benzazepine derivatives for therapeutic purposes.
    本发明涉及式(I)的苯并氮杂环衍生物或其生理耐受盐。本发明还涉及包含这种苯并氮杂环衍生物的药物组合物,以及利用这种苯并氮杂环衍生物进行治疗目的的用途。
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