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potassium methaneselenolate | 54196-34-8

中文名称
——
中文别名
——
英文名称
potassium methaneselenolate
英文别名
methaneselenol; potassium salt;methylselanylpotassium
potassium methaneselenolate化学式
CAS
54196-34-8
化学式
CH3Se*K
mdl
——
分子量
133.093
InChiKey
JFZIVHYRKQFNQL-UHFFFAOYSA-M
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):
    -0.18
  • 重原子数:
    3
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    potassium methaneselenolatediborane(6) 作用下, 以 xylene 为溶剂, 生成 methylselanyl-diborane(6)
    参考文献:
    名称:
    Potassium bisboranemethylselenide(1-) and .mu.-methylselenodiborane
    摘要:
    DOI:
    10.1021/ja00829a075
  • 作为产物:
    描述:
    二甲基二硒醚一水合肼 、 potassium hydroxide 作用下, 反应 2.5h, 生成 potassium methaneselenolate
    参考文献:
    名称:
    Reactions of chloromethyl heptyl ether with selenium and tellurium in the system hydrazine hydrate-potassium hydroxide
    摘要:
    Chloromethyl heptyl ether reacts with selenium in the system hydrazine hydrate-potassium hydroxide with formation of a mixture of bis(heptyloxymethyl)selane (32%) and bis(heptyloxymethyl)diselane (64%). Reductive cleavage of the latter with hydrazine hydrate-KOH and subsequent alkylation with methyl iodide gave methyl(heptyloxymethyl) selane in 94% yield. Analogous reaction of tellurium with hydrazine hydrate-KOH leads to the formation of extremely unstable bis(heptyloxymethyl) ditellane and bis(heptyloxymethyl) tellane at a ratio of 1 : 4.
    DOI:
    10.1134/s1070428011120049
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文献信息

  • Ende,D.V. et al., Angewandte Chemie, 1975, vol. 87, p. 709 - 710
    作者:Ende,D.V. et al.
    DOI:——
    日期:——
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: B: B-Verb.3, 4.7, page 82 - 86
    作者:
    DOI:——
    日期:——
  • New approaches to synthesis of unsaturated organochalcogen compounds with two different chalcogen atoms
    作者:E. P. Levanova、V. S. Vakhrina、V. A. Grabel’nykh、I. B. Rozentsveig、N. V. Russavskaya、A. I. Albanov、E. R. Sanzheeva、N. A. Korchevin
    DOI:10.1134/s1070363214110152
    日期:2014.11
    Two approaches to synthesis of bis-chalcogenyl derivatives of propene with two different chalcogen atoms are proposed. Reaction of 2,3-dichloro-1-propene with two different chalcogen nucleophiles PhY- (Y = S, Se) results in a mixture of two products with two identical chalcogen atoms and two products with different ones. The reactivity of PhY- anions under the reaction conditions (60A degrees C) practically does not depend on the Y nature. Reaction of anions RY- (Y = S, Se, Te) with the products of the reaction of 2,3-dichloro-1-propene and organic chalcogenides in the hydrazine hydrate-alkali medium affords the target unsaturated chalcogen-containing compounds with two different chalcogen atoms, 1,2-bis(organylchalcogenyl) propenes in up to 73% yield.
  • Synthesis of unsaturated organoselenium compounds via the reaction of organic diselenides with 2,3-dichloro-1-propene in the hydrazine hydrate-KOH system
    作者:E. P. Levanova、V. A. Grabel’nykh、V. S. Vakhrina、N. V. Russavskaya、A. I. Albanov、L. V. Klyba、O. A. Tarasova、I. B. Rozentsveig、N. A. Korchevin
    DOI:10.1134/s1070363213090065
    日期:2013.9
    Dimethyldiselenide reacts with 2,3-dichloro-1-propene at 20-25A degrees C in the hydrazine hydrate-KOH medium to form 2-chloro-3-methylselanyl-1-propene with 90% yield. Diphenyldiselenide in the reaction with 2,3-dichloro-1-propene, depending on the conditions, can give quite selectively four products: 2-chloro-3-phenylselanyl-1-propene, phenylselanylpropadiene, 1-phenylselanyl-1-propyne, and Z-1,2-bis(phenylselanyl)-1-propene. The effect of the selenium atom on the reaction direction and the products structure is discussed.
  • POTAPOV, V. A.;AMOSOVA, S. V.;DENISOV, A. L., ZH. ORGAN. XIMII, 25,(1989) N, S. 1112-1113
    作者:POTAPOV, V. A.、AMOSOVA, S. V.、DENISOV, A. L.
    DOI:——
    日期:——
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