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2-(4-piperidin-1-yl-phenyl)-propan-2-ol | 52414-60-5

中文名称
——
中文别名
——
英文名称
2-(4-piperidin-1-yl-phenyl)-propan-2-ol
英文别名
α,α-Dimethyl-p-piperidino-benzylalkohol;BENZYL ALCOHOL, alpha,alpha-DIMETHYL-4-PIPERIDINO-;2-(4-piperidin-1-ylphenyl)propan-2-ol
2-(4-piperidin-1-yl-phenyl)-propan-2-ol化学式
CAS
52414-60-5
化学式
C14H21NO
mdl
——
分子量
219.327
InChiKey
JGTLMSXILSHCMY-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

  • 熔点:
    72-74 °C(Solv: ligroine (8032-32-4))
  • 沸点:
    366.7±25.0 °C(Predicted)
  • 密度:
    1.047±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    23.5
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933399090

SDS

SDS:1696292e4c96deb726f5495646ba5387
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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:
    2-(4-piperidin-1-yl-phenyl)-propan-2-ol盐酸 作用下, 以 丙酮 为溶剂, 反应 1.0h, 以70%的产率得到1-(p-isopropenylphenyl)piperidine
    参考文献:
    名称:
    A new paradigm for biohydroxylation by Beauveria bassiana ATCC 7159
    摘要:
    The biohydroxylation of a series of amides and related amino, keto and hydrocarbon substrates by the fungal biocatalyst Beauveria bassiana ATCC 7159 has been examined. The product distributions, together with data obtained from selective inhibition experiments using the cyt.P-450 inhibitors isosafrole, 1-aminobenzotriazole and phenylacetylene, suggest that B. bassiana contains a range of hydroxylase enzymes with different substrate specificities. A paradigm is presented for the interpretation of the results of microbial hydroxylation and for the application of existing active site models for B. bassiana. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00393-2
  • 作为产物:
    描述:
    4-哌啶苯乙酮甲基溴化镁乙醚 为溶剂, 以86%的产率得到2-(4-piperidin-1-yl-phenyl)-propan-2-ol
    参考文献:
    名称:
    A new paradigm for biohydroxylation by Beauveria bassiana ATCC 7159
    摘要:
    The biohydroxylation of a series of amides and related amino, keto and hydrocarbon substrates by the fungal biocatalyst Beauveria bassiana ATCC 7159 has been examined. The product distributions, together with data obtained from selective inhibition experiments using the cyt.P-450 inhibitors isosafrole, 1-aminobenzotriazole and phenylacetylene, suggest that B. bassiana contains a range of hydroxylase enzymes with different substrate specificities. A paradigm is presented for the interpretation of the results of microbial hydroxylation and for the application of existing active site models for B. bassiana. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00393-2
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文献信息

  • HICKS T. A.; SMITH C. E.; WILLIAMSON W. R. N.; DAY E. H., J. MED. CHEM., 1979, 22, NO 12, 1460-1464
    作者:HICKS T. A.、 SMITH C. E.、 WILLIAMSON W. R. N.、 DAY E. H.
    DOI:——
    日期:——
  • A new paradigm for biohydroxylation by Beauveria bassiana ATCC 7159
    作者:Herbert L Holland、Terence A Morris、Phillip J Nava、Mirjana Zabic
    DOI:10.1016/s0040-4020(99)00393-2
    日期:1999.6
    The biohydroxylation of a series of amides and related amino, keto and hydrocarbon substrates by the fungal biocatalyst Beauveria bassiana ATCC 7159 has been examined. The product distributions, together with data obtained from selective inhibition experiments using the cyt.P-450 inhibitors isosafrole, 1-aminobenzotriazole and phenylacetylene, suggest that B. bassiana contains a range of hydroxylase enzymes with different substrate specificities. A paradigm is presented for the interpretation of the results of microbial hydroxylation and for the application of existing active site models for B. bassiana. (C) 1999 Elsevier Science Ltd. All rights reserved.
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