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9-甲基腺嘌呤-d3 | 130859-46-0

中文名称
9-甲基腺嘌呤-d3
中文别名
——
英文名称
9-Methyl-d3 Adenine
英文别名
9-(trideuteriomethyl)purin-6-amine
9-甲基腺嘌呤-d3化学式
CAS
130859-46-0
化学式
C6H7N5
mdl
——
分子量
152.131
InChiKey
WRXCXOUDSPTXNX-FIBGUPNXSA-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:
    272-274°C
  • 溶解度:
    溶于甲醇、水

计算性质

  • 辛醇/水分配系数(LogP):
    0
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    69.6
  • 氢给体数:
    1
  • 氢受体数:
    4

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

反应信息

  • 作为产物:
    参考文献:
    名称:
    Surface-enhanced Raman scattering study on adsorption structures of 9-methyladenine at silver electrode surfaces
    摘要:
    Surface-enhanced Raman scattering (SERS) spectra are measured for 9-methyladenine (9-MA), its N1-protonated form (9-MAH+), and the deuterated analogues of 9-MAH+ adsorbed on silver electrodes as a function of pH and electrode potential (E). The surface spectra observed for the adsorbate on the electrode in 0.1 mol/L KCl at E = 0.2 V (vs Ag/AgCl) and at pH values 2.8 and 1.0 prove that the adsorbate exists as the protonated form taking a nearly flat orientation to the electrode surface. When E is stepped to -0.4 V at pH 2.8, the adsorbate is converted to 9-MA with an end-on orientation; thus, the potential sweep results in a deprotonation process as well as an orientational change. At E = -0.2 V the coadsorbed chloride ions neutralize the positive charge of the adsorbate and stabilize the protonated form on the surface; on stepping E to -0.4 V, the chloride ions are desorbed from the surface, resulting in the increase in an electrostatic interaction between the adsorbate and the electrode surface; the increase causes the deprotonation. On the other hand, when E is swept from -0.2 to -0.4 V at pH 1.0, the adsorbate, which keeps the protonated state taking on a flat orientation to the surface, gives rise to prominent bands due to a C8-H out-of-plane bending (1033 cm-1) and a CH3 out-of-plane rocking (953 cm-1) vibration. The protonated species is more stable at pH 1.0 than the species at pH 2.8, and consequently the desorption of the chloride ions does not cauuse the deprotonation but induces a direct interaction between the adsorbate and the surface, which gives rise to the prominent out-of-lane vibrations.
    DOI:
    10.1021/j100156a057
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文献信息

  • Surface-enhanced Raman scattering study on adsorption structures of 9-methyladenine at silver electrode surfaces
    作者:Koichi Itoh、Keiji Minami、Toshibumi Tsujino、Munsok Kim
    DOI:10.1021/j100156a057
    日期:1991.2
    Surface-enhanced Raman scattering (SERS) spectra are measured for 9-methyladenine (9-MA), its N1-protonated form (9-MAH+), and the deuterated analogues of 9-MAH+ adsorbed on silver electrodes as a function of pH and electrode potential (E). The surface spectra observed for the adsorbate on the electrode in 0.1 mol/L KCl at E = 0.2 V (vs Ag/AgCl) and at pH values 2.8 and 1.0 prove that the adsorbate exists as the protonated form taking a nearly flat orientation to the electrode surface. When E is stepped to -0.4 V at pH 2.8, the adsorbate is converted to 9-MA with an end-on orientation; thus, the potential sweep results in a deprotonation process as well as an orientational change. At E = -0.2 V the coadsorbed chloride ions neutralize the positive charge of the adsorbate and stabilize the protonated form on the surface; on stepping E to -0.4 V, the chloride ions are desorbed from the surface, resulting in the increase in an electrostatic interaction between the adsorbate and the electrode surface; the increase causes the deprotonation. On the other hand, when E is swept from -0.2 to -0.4 V at pH 1.0, the adsorbate, which keeps the protonated state taking on a flat orientation to the surface, gives rise to prominent bands due to a C8-H out-of-plane bending (1033 cm-1) and a CH3 out-of-plane rocking (953 cm-1) vibration. The protonated species is more stable at pH 1.0 than the species at pH 2.8, and consequently the desorption of the chloride ions does not cauuse the deprotonation but induces a direct interaction between the adsorbate and the surface, which gives rise to the prominent out-of-lane vibrations.
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