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N-(2-hydroxy-1-naphthylidene)-1-butylamine | 31012-22-3

中文名称
——
中文别名
——
英文名称
N-(2-hydroxy-1-naphthylidene)-1-butylamine
英文别名
N-n-butyl-2-hydroxy-1-naphthaldimine;Butyl-<2-hydroxy-naphthyl-(1)-methylen>-amin;2-Hydroxy-1-naphthyliden-n-butylamin;2-Hydroxy-naphthaldehyd-butylimin;1-(Butyliminomethyl)naphthalen-2-ol
N-(2-hydroxy-1-naphthylidene)-1-butylamine化学式
CAS
31012-22-3
化学式
C15H17NO
mdl
——
分子量
227.306
InChiKey
RSERDUBQTCJWPW-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

  • 沸点:
    386.3±25.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    32.6
  • 氢给体数:
    1
  • 氢受体数:
    2

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

点击查看最新优质反应信息

文献信息

  • The Preparation and Characterization of Dichloromanganese(IV) Schiff Base Complexes
    作者:Takayuki Matsushita、Hiroshi Kono、Toshiyuki Shono
    DOI:10.1246/bcsj.54.2646
    日期:1981.9
    oxidation state of the manganese ions in these complexes is +IV. The electronic spectra show an intense band around 16000 cm−1 which can be assigned to a charge-transfer transition. In the cyclic voltammograms, two cathodic waves are observed at half-peak potentials around +0.9 V and −0.2 V(vs. SCE); they can be assigned to the reductions of Mn(IV) to Mn(III) and of Mn(III) to Mn(II) respectiv...
    一些 (III) 席夫碱配合物与氯化氢反应生成深绿色配合物,其经验式为 MnLCl2 或 MnL'2Cl2,其中 H2L 表示四齿配体,如 N,N'-二杨基乙二胺及其类似物,其中 HL' 表示双齿配体,如 N-丁基杨烯胺及其类似物。这些配合物是乙腈中的非电解质。它们在室温下的磁矩在 3.9 到 4.1 BM 范围内,并且在 77 到 300 K 的温度范围内,磁化率服从居里-魏斯定律,θ 值很小,表明锰离子在这些复合物是+IV。电子光谱在 16000 cm-1 附近显示出一个强带,可以将其指定为电荷转移跃迁。在循环伏安图中,在 +0.9 V 和 -0.2 V(vs. SCE)附近的半峰电位处观察到两个阴极波;它们可以分别归因于 Mn(IV) 到 Mn(III) 和 Mn(III) 到 Mn(II) 的还原……
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: U: SVol.E2, 1.7.5, page 60 - 104
    作者:
    DOI:——
    日期:——
  • Structures and properties of di-μ-oxo dimanganese(IV) complexes with bidentate Schiff bases, N-alkyl-substituted-salicylideneamine
    作者:Hitoshi Torayama、Hideyuki Asada、Manabu Fujiwara、Takayuki Matsushita
    DOI:10.1016/s0277-5387(98)00144-2
    日期:1998.11
    Novel di-mu-oxo dimanganese(IV) complexes, [Mn-IV(N-R-X-sal)(2)(mu-O)](2), with bidentate Schiff base ligands, N-alkyl-substituted-salicylideneamine, N-R-X-salH [R= CH3(Me), C2H5 (Et), n-C3H, (Pr), n-C4H9 (Bu), n-C6H13 (Hx), n-C8H17 (Oct), II-C10H21 (Dec), n-C12H25 (Dod), or n-C18H37 (Octd) and X = H or 5,6-benzo]: have been prepared by their reaction with potassium permanganate (KMnO4) in MeCN, while stirring at room temperature. These complexes were characterized by spectroscopy, magnetic susceptibility, thermal analysis and X-ray crystallography. The structures consist of a Mn-2(IV)(mu-O)(2) core with a Mn-Mn separation of 2.731 (4) Angstrom for [Mn-IV(N-Me-sal)(2)(mu-O)](2), 1, 2.769(2) Angstrom for [Mn-2(IV)(N-Et-sal)(2)(mu-O)](2), 2, 2.780(2) Angstrom for [(Mn-IV-Hx-sal)(2)(mu-O)](2), 5, 2.780(2)Angstrom for [Mn-IV(N-Dec-sal)(2)(mu-O)](2), 7, and 2.756(3) Angstrom for [Mn-IV(N-Me-5,6-benzo-sal)(2)(mu-O)](2), 10. The complex 1 is the first di-mu-oxo dimanganese(IV) complex having asymmetrical form in which two manganese ions adopt different configurations each other. Moreover, the complexes 5 and 7 are found to exhibit the longest one among all of the Mn-Mn separation observed for the structurally characterized Mn-2(mu-O)(2) complexes prior to this work. The antiferromagnetic exchange interaction has been found to be J= -83 and -188 cm(-1) for 1 and 7, respectively. (C) 1998 Elsevier Science Ltd. All rights reserved.
  • Schiff base complexes of dioxouranium(VI)-(IV) dioxouranium(VI) chloride complexes with monobasic bidentate Schiff bases
    作者:R.G. Vijay、J.P. Tandon
    DOI:10.1016/0022-1902(77)80360-6
    日期:1977.1
  • Yamada, S.; Takeuchi, A., Bulletin of the Chemical Society of Japan, 1969, vol. 42, p. 2549 - 2551
    作者:Yamada, S.、Takeuchi, A.
    DOI:——
    日期:——
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