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N,4-diphenyl-1,3-oxazol-2-amine | 72546-32-8

中文名称
——
中文别名
——
英文名称
N,4-diphenyl-1,3-oxazol-2-amine
英文别名
phenyl-(4-phenyl-oxazol-2-yl)-amine;2-Phenylamino-4-phenyloxazol
N,4-diphenyl-1,3-oxazol-2-amine化学式
CAS
72546-32-8
化学式
C15H12N2O
mdl
——
分子量
236.273
InChiKey
ONKIQOMZWLQXIO-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):
    3.9
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    38.1
  • 氢给体数:
    1
  • 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

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文献信息

  • Ultrasound and deep eutectic solvent (DES): A novel blend of techniques for rapid and energy efficient synthesis of oxazoles
    作者:Balvant S. Singh、Hyacintha R. Lobo、Dipak V. Pinjari、Krishna J. Jarag、Aniruddha B. Pandit、Ganapati S. Shankarling
    DOI:10.1016/j.ultsonch.2012.06.003
    日期:2013.1
    The present work deals with the synthesis of novel oxazole compounds by using effective combination of ultrasound (US) and deep eutectic solvent (DES). The reaction was also conducted by thermal method (NUS) and the comparative studies are provided. It was observed that applying ultrasound not only improved yields and reduced reaction times but also saved more than 85% energy as shown by energy consumption calculations. The advantages of using DES as reaction medium is highlighted from the fact that it is bio-degradable, non-toxic, recyclable and could be easily prepared using inexpensive raw materials. The recyclability for DES was studied wherein it was found that ultrasound has no negative effects on DES even up to four runs. In addition, the present work is the first report on the combinative use of DES and US in organic synthesis. (C) 2012 Elsevier B.V. All rights reserved.
  • PATTANAYAK B. K.; ROUT D. N.; NATH J. P.; MAHAPATRA G. N., INDIAN J. CHEM., 1979, B18, NO 3, 286-289
    作者:PATTANAYAK B. K.、 ROUT D. N.、 NATH J. P.、 MAHAPATRA G. N.
    DOI:——
    日期:——
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