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甲基N-异丁酰基-N-甲基甘氨酸酯 | 445396-08-7

中文名称
甲基N-异丁酰基-N-甲基甘氨酸酯
中文别名
甘氨酸,N-甲基-N-(2-甲基-1-羰基丙基)-,甲基酯
英文名称
methyl N-methyl-N-(2-methylpropanoyl)glycinate
英文别名
Glycine, N-methyl-N-(2-methyl-1-oxopropyl)-, methyl ester;methyl 2-[methyl(2-methylpropanoyl)amino]acetate
甲基N-异丁酰基-N-甲基甘氨酸酯化学式
CAS
445396-08-7
化学式
C8H15NO3
mdl
MFCD12144782
分子量
173.212
InChiKey
UDAFIYUWJLPNJI-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:
    12
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:f0029297cf032877bef402196cf89a36
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反应信息

  • 作为反应物:
    描述:
    甲基N-异丁酰基-N-甲基甘氨酸酯劳森试剂 作用下, 以 甲苯 为溶剂, 反应 3.0h, 以89%的产率得到methyl N-methyl-N-(2-methylpropanethioyl)glycinate
    参考文献:
    名称:
    Synthesis and Use of 2H-Azirin-3-amines as Dipeptide Synthons
    摘要:
    The synthesis of the new 2H-azirin-3-amines ('3-amino-2H-azirines') 11, 20, 28, and 33 as dipeptide synthons is described. The reactions of the starting amides with Lawesson reagent gave the corresponding thioamides, and consecutive treatment with COCl2, 1,4-diazabicyclo[2.2.2]octane (DABCO), and NaN3 led to the desired products. It is shown that these 2H-azirin-3-amines can conveniently be used as building blocks of the dipeptides Aib-(Me)Axx (Axx = alanine, valine), Aib-Homoproline, and Iva-Pro in the synthesis of several model peptides. However, some limitations apply for the synthesis of such 2H-azirin-3-amines. The starting material for the azirine synthesis, the corresponding thioamides, cannot generally be synthesized, and the 2H-azirin-3-amines could not be obtained in all cases from the thioamides prepared.
    DOI:
    10.1002/1522-2675(200203)85:3<885::aid-hlca885>3.0.co;2-z
  • 作为产物:
    描述:
    肌氨酸甲酯盐酸盐异丁酰氯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 1.92h, 以77%的产率得到甲基N-异丁酰基-N-甲基甘氨酸酯
    参考文献:
    名称:
    Synthesis and Use of 2H-Azirin-3-amines as Dipeptide Synthons
    摘要:
    The synthesis of the new 2H-azirin-3-amines ('3-amino-2H-azirines') 11, 20, 28, and 33 as dipeptide synthons is described. The reactions of the starting amides with Lawesson reagent gave the corresponding thioamides, and consecutive treatment with COCl2, 1,4-diazabicyclo[2.2.2]octane (DABCO), and NaN3 led to the desired products. It is shown that these 2H-azirin-3-amines can conveniently be used as building blocks of the dipeptides Aib-(Me)Axx (Axx = alanine, valine), Aib-Homoproline, and Iva-Pro in the synthesis of several model peptides. However, some limitations apply for the synthesis of such 2H-azirin-3-amines. The starting material for the azirine synthesis, the corresponding thioamides, cannot generally be synthesized, and the 2H-azirin-3-amines could not be obtained in all cases from the thioamides prepared.
    DOI:
    10.1002/1522-2675(200203)85:3<885::aid-hlca885>3.0.co;2-z
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文献信息

  • USE OF SUBSTITUTED 1-(ARYL ETHYNYL)-, 1-(HETEROARYL ETHYNYL)-, 1-(HETEROCYCLYL ETHYNYL)- AND 1-(CYCLOALKENYL ETHYNYL)-CYCLOHEXANOLS AS ACTIVE AGENTS AGAINST ABIOTIC PLANT STRESS
    申请人:BAYER CROPSCIENCE AG
    公开号:US20150305334A1
    公开(公告)日:2015-10-29
    The invention relates to the use of substituted 1-(arylethynyl)-, 1-(heteroarylethynyl)-, 1-(heterocyclylethynyl)- and 1-(cycloalkenylethynyl)cyclohexanols or salts thereof where the radicals in the general formula (I) correspond to the definitions given in the description, for enhancing stress tolerance in plants to abiotic stress and/or for increasing plant yield.
    本发明涉及使用取代的1-(芳基乙炔基)-、1-(杂芳基乙炔基)-、1-(杂环基乙炔基)-和1-(环烯基乙炔基)环己醇或其盐,其中通式(I)中的基团与描述中给定的定义相对应,用于增强植物对非生物胁迫的耐受性和/或增加植物产量。
  • USE OF SUBSTITUTED 1-(ARYL ETHYNYL)-, 1-(HETEROARYL ETHYNYL)-, 1-(HETEROCYCLYL ETHYNYL)- AND 1-(CYCLOALKENYLETHYNYL)-BICYCLOALKANOLS AS ACTIVE AGENTS AGAINST ABIOTIC PLANT STRESS
    申请人:BAYER CROPSCIENCE AG
    公开号:US20150315146A1
    公开(公告)日:2015-11-05
    The invention relates to the use of substituted 1-(arylethynyl)-, 1-(heteroarylethynyl)-, 1-(heterocyclylethynyl)- and 1-(cycloalkenylethynyl)bicycloalkanols or salts thereof where the radicals in the general formula (I) correspond to the definitions given in the description, for enhancing stress tolerance in plants to abiotic stress and/or for increasing plant yield.
    该发明涉及使用取代的1-(芳基乙炔基)-、1-(杂芳基乙炔基)-、1-(杂环基乙炔基)-和1-(环烯基乙炔基)双环戊醇或其盐,其中一般式(I)中的基团对应于描述中给定的定义,用于增强植物对非生物胁迫的耐受性和/或增加植物产量。
  • Synthesis and Use of 2H-Azirin-3-amines as Dipeptide Synthons
    作者:Roland A. Breitenmoser、Heinz Heimgartner
    DOI:10.1002/1522-2675(200203)85:3<885::aid-hlca885>3.0.co;2-z
    日期:2002.3
    The synthesis of the new 2H-azirin-3-amines ('3-amino-2H-azirines') 11, 20, 28, and 33 as dipeptide synthons is described. The reactions of the starting amides with Lawesson reagent gave the corresponding thioamides, and consecutive treatment with COCl2, 1,4-diazabicyclo[2.2.2]octane (DABCO), and NaN3 led to the desired products. It is shown that these 2H-azirin-3-amines can conveniently be used as building blocks of the dipeptides Aib-(Me)Axx (Axx = alanine, valine), Aib-Homoproline, and Iva-Pro in the synthesis of several model peptides. However, some limitations apply for the synthesis of such 2H-azirin-3-amines. The starting material for the azirine synthesis, the corresponding thioamides, cannot generally be synthesized, and the 2H-azirin-3-amines could not be obtained in all cases from the thioamides prepared.
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同类化合物

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