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2-methoxy-4-acetoxy-6-methyl pyrimidine | 100936-10-5

中文名称
——
中文别名
——
英文名称
2-methoxy-4-acetoxy-6-methyl pyrimidine
英文别名
2-Methoxy-6-methyl-4-pyrimidinyl acetate;(2-methoxy-6-methylpyrimidin-4-yl) acetate
2-methoxy-4-acetoxy-6-methyl pyrimidine化学式
CAS
100936-10-5
化学式
C8H10N2O3
mdl
——
分子量
182.179
InChiKey
LLIBHMVCSPALMG-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

  • 熔点:
    121-122 °C(Solv: chloroform (67-66-3))
  • 沸点:
    299.0±32.0 °C(Predicted)
  • 密度:
    1.184±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    61.3
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:5a4bd460b9246f91fcef1fb36276c5bb
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反应信息

  • 作为反应物:
    描述:
    2-methoxy-4-acetoxy-6-methyl pyrimidine正丁醇 以10%的产率得到乙酸丁酯
    参考文献:
    名称:
    嘧啶转化中的6-烷基-2-乙氧基-4-(3h)-嘧啶酮:4-酰化嘧啶衍生物的区域特异性制备,抗肿瘤和抗菌活性。胺选择性酰化的新剂
    摘要:
    提出了4-酰化吡咯烷基的高产率合成。这些产品是胺酰基乙酰胺的选择性试剂。抗肿瘤和化合物的抗微生物活性和还报道。
    DOI:
    10.1016/0040-4039(88)85275-4
  • 作为产物:
    描述:
    6-methyl-2-methoxy-4-O-piperonylpyrimidine 在 吡啶 作用下, 以 乙腈 为溶剂, 反应 24.0h, 生成 2-methoxy-4-acetoxy-6-methyl pyrimidine
    参考文献:
    名称:
    Researches on antiviral agents. 4. Studies on the chemistry of 6-methyl-2-methoxy-4-O-acyloxy and 6-methyl-2,4-di-O-acyloxypyrimidine derivatives as new acylation reagents and inhibitors of uracil DNA glycosylases.
    摘要:
    The synthesis of 6-methyl-2-methoxy-4-O-acyloxy and 6-methyl-2,4-di-O-acyloxypyrimidine derivatives 2 and 5 along with their properties as acylating agents of amines, alcohols, thiols and alpha-amino acids have been reported. Interestingly some of the tide products revealed an inhibitory activity against the human and herpetic DNA glycosylases.
    DOI:
    10.1016/s0040-4020(01)87037-x
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文献信息

  • 6-alkyl- and 5,6-dialkyl-2-methoxy-4(3H)-pyrimidinones in the transformations of pyrimidines. Regiospecific 1--acylation of pyrimidines.
    作者:Maurizio Botta、Francesco De Angelis、Gabriella Finizia、Rosario Nicoletti、Maurizio Delfini
    DOI:10.1016/s0040-4039(00)98294-7
    日期:1985.1
  • Botta Maurizio, Saladino Raffaele, Gentile Gabriella, Summa Vincenzo, Nic+, Tetrahedron, 50 (1994) N 11, S 3603-3618
    作者:Botta Maurizio, Saladino Raffaele, Gentile Gabriella, Summa Vincenzo, Nic+
    DOI:——
    日期:——
  • BOTTA, MAURIZIO;DE, ANGELIS FRANCESCO;NICOLETTI, ROSARIO, TETRAHEDRON LETT., 29,(1988) N 22, 2741-2744
    作者:BOTTA, MAURIZIO、DE, ANGELIS FRANCESCO、NICOLETTI, ROSARIO
    DOI:——
    日期:——
  • Researches on antiviral agents. 4. Studies on the chemistry of 6-methyl-2-methoxy-4-O-acyloxy and 6-methyl-2,4-di-O-acyloxypyrimidine derivatives as new acylation reagents and inhibitors of uracil DNA glycosylases.
    作者:Maurizio Botta、Raffaele Saladino、Gabriella Gentile、Vincenzo Summa、Rosario Nicoletti、Annalisa Verri、Federico Focher、Silvio Spadari
    DOI:10.1016/s0040-4020(01)87037-x
    日期:1994.3
    The synthesis of 6-methyl-2-methoxy-4-O-acyloxy and 6-methyl-2,4-di-O-acyloxypyrimidine derivatives 2 and 5 along with their properties as acylating agents of amines, alcohols, thiols and alpha-amino acids have been reported. Interestingly some of the tide products revealed an inhibitory activity against the human and herpetic DNA glycosylases.
  • 6-alkyl-2-hethoxy-4-(3h)-pyrimidinones in the transformation of pyrimidines: regiospecific preparation, antitumor and antimicrobial activity of 4-O-acylated pyrimidine derivatives. New agents for selective acylation of amines
    作者:Maurizio Botta、Francesco De Angelis、Rosarlo Nicoletti、Alessandra Pani、Maria Elena Marongiu、Paolo La Colla
    DOI:10.1016/0040-4039(88)85275-4
    日期:——
    A high yielding synthesis of 4--acylated pyrlmldines is presented. These products are selective reagents for amine acylatlon. The antitumor and antimicrobial activity of compounds and is also reported.
    提出了4-酰化吡咯烷基的高产率合成。这些产品是胺酰基乙酰胺的选择性试剂。抗肿瘤和化合物的抗微生物活性和还报道。
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