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2-羟基-2,3-二甲基丁酰胺 | 66461-67-4

中文名称
2-羟基-2,3-二甲基丁酰胺
中文别名
——
英文名称
2-hydroxy-2,3-dimethyl-butyric acid amide
英文别名
2-Hydroxy-2,3-dimethyl-buttersaeure-amid;2.3.3-Trimethyl-milchsaeure-amid;2-Hydroxy-2,3-dimethyl-butyramid;2-Hydroxy-2-methylisovaleramid;2-Hydroxy-2,3-dimethylbutanamide
2-羟基-2,3-二甲基丁酰胺化学式
CAS
66461-67-4
化学式
C6H13NO2
mdl
——
分子量
131.175
InChiKey
ZETNTQRARNBFOL-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
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    63.3
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:f729f906d7350dc5f673549d6bef5098
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反应信息

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文献信息

  • COFERONS AND METHODS OF MAKING AND USING THEM
    申请人:Barany Francis
    公开号:US20120295874A1
    公开(公告)日:2012-11-22
    The present invention is directed to a monomer useful in preparing therapeutic compounds. The monomer includes one or more pharmacophores which potentially binds to a target molecule with a dissociation constant of less than 300 μM and a linker element connected to the pharmacophore. The linker element has a molecular weight less than 500 daltons, is connected, directly or indirectly through a connector, to the pharmacophore.
    本发明涉及一种用于制备治疗性化合物的单体。该单体包括一个或多个可与目标分子结合的药效团,其解离常数小于300微摩尔,以及与药效团连接的连接元素。所述连接元素的分子量小于500道尔顿,通过直接连接或通过连接器间接与药效团相连。
  • Aryl Substituted Indoles and Their Use as Blockers of Sodium Channels
    申请人:Kyle Donald J.
    公开号:US20130296281A1
    公开(公告)日:2013-11-07
    The invention relates to aryl and heteroaryl substituted compounds of Formula (I), and pharmaceutically acceptable salts, prodrugs, or solvates thereof, wherein G, R 1 , and Z 1 -Z 5 are defined as set forth in the specification. The invention is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of sodium channels. Compounds of the present invention are especially useful for treating pain.
    本发明涉及具有式(I)的芳基和杂芳基取代化合物,以及其药学上可接受的盐、前药或溶剂化物,其中G、R1和Z1-Z5如规范中所述。本发明还涉及利用式(I)的化合物治疗对通道阻滞有响应的疾病。本发明的化合物特别适用于治疗疼痛。
  • [EN] METHOD FOR THE MANUFACTURE OF N, N-DIALLKYLLACTAMIDE<br/>[FR] PROCÉDÉ DE PRÉPARATION DE N,N-DIALKYLLACTAMIDE
    申请人:PURAC BIOCHEM BV
    公开号:WO2016050894A1
    公开(公告)日:2016-04-07
    The invention relates to a method for the manufacture of N,N-dialkyllactamide, whereby at least one of the compounds selected from the series consisting of alkyl lactate, lactide and polylactic acid is mixed with dialkylamine in order to form a reaction mixture, under conditions whereby aminolysis takes place in the reaction mixture. The method is characterized in that the reaction mixture further comprises a Lewis acid. As a result of the invented method, N,N-dialkyllactamides can be manufactured in high yields and with high optical purity.
    本发明涉及一种制备N,N-二烷基内酰胺的方法,其中从由烷基乳酸酯、乳酸内酯和聚乳酸组成的系列中至少选择一种化合物与二烷基胺混合,以形成反应混合物,在反应混合物中进行胺解反应。该方法的特征在于,反应混合物还包括一种路易斯酸。由于该发明方法,N,N-二烷基内酰胺可以高产率、高光学纯度地制备。
  • [EN] PROCESS FOR MANUFACTURING N,N-DIALKYL LACTAMIDE<br/>[FR] PROCÉDÉ POUR LA FABRICATION DE N,N-DIALKYLLACTAMIDE
    申请人:PURAC BIOCHEM BV
    公开号:WO2010037776A1
    公开(公告)日:2010-04-08
    The present invention pertains to a process for manufacturing dialkyl lactamide comprising the steps of reacting lactide and dialkylamine selected from one or more of dimethylamine, diethylamine, and methylethylamine to form a reaction mixture which comprises dialkyl lactamide selected from N, N-dimethyl lactamide, N,N-diethyl lactamide, and N,N-methylethyl lactamide, N,N-dialkyl lactoyl lactamide, and dialkylamine, subjecting the reaction mixture to a separation step to form a product stream comprising N,N-dialkyl lactamide, a first recycle stream comprising dialkylamine and a second recycle stream comprising N,N-dialkyl lactoyl lactamide, feeding the recycle streams to the reaction step, and isolating the product stream. The process allows the manufacture of N, N-dimethyl lactamide, N,N-diethyl lactamide, and N,N-methylethyl lactamide on commercial scale.
    本发明涉及一种制造二烷基内酰胺的方法,包括以下步骤:将内酯和二烷基胺(所选自二甲胺二乙胺和甲乙胺)反应,形成反应混合物,其中包括所选自N,N-二甲基内酰胺、N,N-二乙基内酰胺、N,N-甲乙基内酰胺、N,N-二烷基内酰基内酰胺和二烷基胺的二烷基内酰胺;将反应混合物经过分离步骤,形成产品流,其中包括N,N-二烷基内酰胺、第一循环流,包括二烷基胺和第二循环流,包括N,N-二烷基内酰基内酰胺;将循环流送回反应步骤,隔离产品流。该方法允许商业化生产N,N-二甲基内酰胺、N,N-二乙基内酰胺和N,N-甲乙基内酰胺。
  • PROCESS FOR MANUFACTURING N,N-DIALKYL LACTAMIDE
    申请人:PURAC Biochem BV
    公开号:EP2346812A1
    公开(公告)日:2011-07-27
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