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syn-(methyl,hydro)(methyl,iodo)bimane | 181297-97-2

中文名称
——
中文别名
——
英文名称
syn-(methyl,hydro)(methyl,iodo)bimane
英文别名
6-Iodo-1,7-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione
syn-(methyl,hydro)(methyl,iodo)bimane化学式
CAS
181297-97-2
化学式
C8H7IN2O2
mdl
——
分子量
290.06
InChiKey
AULJQCXXRUMZNI-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):
    1.1
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    syn-(methyl,hydro)(methyl,iodo)bimane 在 palladium diacetate N,N-二异丙基乙胺 作用下, 以 乙腈 为溶剂, 反应 20.0h, 生成 syn-(methyl,bromo)bimane
    参考文献:
    名称:
    Bimane Acetylenes and Diacetylenes. Bimanes. 33
    摘要:
    Two series (4,6-dihydro and 4,6-dimethyl) of syn-bimanes [1,5-diazabicyclo[3.3.0]octa-3,6-diene-2,8-diones] have been converted to acetylene and diacetylene derivatives. Their chemical and photophysical properties are reported. The 3-(and 6-)iodo (diiodo) derivatives are the best choices for Stille or Heck condensations with acetylenes or acrylates. Desilylation of (trimethylsilyl)acetylenes is best carried out with silver nitrate followed by lithium bromide. The acetylenes and diacetylenes are quite stable and highly fluorescent and represent candidate units for incorporation into polymers.
    DOI:
    10.1021/jo951830b
  • 作为产物:
    描述:
    syn-(methyl,chloro)bimane 在 palladium on activated charcoal 氢气一氯化碘 作用下, 以 二氯甲烷溶剂黄146 为溶剂, 反应 3.0h, 生成 syn-(methyl,hydro)(methyl,iodo)bimane
    参考文献:
    名称:
    Bimane Acetylenes and Diacetylenes. Bimanes. 33
    摘要:
    Two series (4,6-dihydro and 4,6-dimethyl) of syn-bimanes [1,5-diazabicyclo[3.3.0]octa-3,6-diene-2,8-diones] have been converted to acetylene and diacetylene derivatives. Their chemical and photophysical properties are reported. The 3-(and 6-)iodo (diiodo) derivatives are the best choices for Stille or Heck condensations with acetylenes or acrylates. Desilylation of (trimethylsilyl)acetylenes is best carried out with silver nitrate followed by lithium bromide. The acetylenes and diacetylenes are quite stable and highly fluorescent and represent candidate units for incorporation into polymers.
    DOI:
    10.1021/jo951830b
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同类化合物

溴代双满 6-硝基-2,4-二氢吡唑并[4,3-c]吡唑-3-羧酸 6-甲基-4-(三氟甲基)-1,6-二氢吡唑并[3,4-c]吡唑-3-基胺 5-(溴甲基)-N,N,N,2,6-五甲基-1,7-二氧代-1H,7H-吡唑并[1,2-A]吡唑-3-甲基溴化铵 3-碘-1-(四氢-2H-吡喃-2-基)-1H-吡唑并[4,3-B]吡啶 3-硝基-1,4-二氢吡唑并[4,3-c]吡唑 3-(溴甲基)-2,6,7-三甲基-1H,5H-吡唑并[1,2-a]吡唑-1,5-二酮 3,5-双溴甲基-2,6-二甲基吡唑并[1,2-a]吡唑-1,7-二酮 2,3,6-三甲基-5-[(2-吡啶基二硫代)甲基]-1H,7H-吡唑并[1,2-a]吡唑-1,7-二酮 2,3,6,7-四甲基-1,5-二氮杂双环[3.3.0]-2,6-辛二烯-4,8-二酮 2,3,5,6-四甲基-1H,7H-吡唑并[1,2-a]吡唑-1,7-二酮 9,10-dioxa-μ-methylthianio-syn-(methylene,methyl)bimane fluorosulfate 9,10-dioxa-anti-(bromomethyl,methyl)bimane 9,10-dioxa-syn-(hydrogen,bromo)bimane 9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 4,6-(1,4-tetramethylene)-3,7-dichloro-1,5-diazabicyclo<3.3.0>octa-3,6-diene-2,8-dione 9,10-dioxa-syn-(1-propylthiomethyl,methyl)bimane 9,10-dioxa-μ-tert-butylimino-syn-(methylene,methyl)bimane 9,10-dioxa-anti-(methyl,methyl)(methy,bromo)bimane 9,10-dioxa-syn-(fluoromethyl,methyl)(methyl,methyl)bimane 9,10-dioxa-syn-(trimethylammoniomethyl,methyl)(methyl,methyl)bimane bromide 9,10-dioxa-syn-(piperidinomethyl,methyl)bimane 9,10-dioxa-syn-(N-phenyl-N-methylaminomethyl,methyl)bimane 9,10-dioxa-syn-(trimethylammoniomethyl,methyl)bimane dibromide 9,10-dioxa-syn-(methylthiomethyl,methyl)bimane 9,10-dioxa-syn-(chloromethyl,methyl)bimane 9,10-dioxa-syn-(dimethylaminomethyl,methyl)bimane 9,10-dioxa-syn-(methoxymethyl,methyl)bimane (E)-1,4-dihydro-4-(nitromethylene)-1,2,5-trimethylpyridine syn-(methyl,hydro)(methyl,iodo)bimane 9,10-dioxa-μ-acetylimino-syn-(methylene,methyl)bimane 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-4-ium-6-yl acetate;bromide 6-Chloro-1,2,5-trimethylpyrazolo[1,2-a]pyrazole-3,7-dione 3-Bromomethyl-5-hydroxymethyl-2,6-dimethyl-pyrazolo[1,2-a]pyrazole-1,7-dione syn-(methyl,iodo)bimane 1,7-bis(ethenyl)-2,6-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione 9,10-dioxa-syn-(ethyl,chloro)bimane 9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 9,10-dioxa-anti-(hydroxymethyl,methyl)(methyl,methyl)bimane dl-9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 1-(4-ethylsulfanyl-4H-pyridin-1-yl)-2,6-dimethylpyridin-4-one 3-Bromomethyl-5-ethyl-2,6-dimethyl-pyrazolo[1,2-a]pyrazole-1,7-dione 9,10-dioxa-anti-(chloromethyl,methyl)bimane 9,10-dioxa-μ-imino-syn-(methylene,methyl)bimane N,N-Dimethyl-2-nitro-2-(2H-tetrazol-5-yl)-1,1-ethenediamine 1-hydroxy-3,5-diiodo-4,6-dimethyl-1H-pyridin-2-one 9,10-dioxa-anti-(ethyl,chloro)bimane 2,6-dichloro-7-ethenyl-1-ethylpyrazolo[1,2-a]pyrazole-3,5-dione 2,6-dimethyl-3,5-dioxo-4,13-diazatricyclo[5.5.1.04,13]trideca-1,6-diene-10-carboxylic acid ethyl 2,6-dimethyl-3,5-dioxo-4,13-diazatricyclo[5.5.1.04,13]trideca-1,6-diene-10-carboxylate