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3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-(3-phenylpropyl)-4-piperidinol | 70151-95-0

中文名称
——
中文别名
——
英文名称
3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-(3-phenylpropyl)-4-piperidinol
英文别名
3-[2-hydroxy-4-(2-methyloctan-2-yl)phenyl]-4-(3-phenylpropyl)piperidin-4-ol
3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-(3-phenylpropyl)-4-piperidinol化学式
CAS
70151-95-0
化学式
C29H43NO2
mdl
——
分子量
437.666
InChiKey
DWJXCHZMHSOWHX-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):
    7.6
  • 重原子数:
    32
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    52.5
  • 氢给体数:
    3
  • 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

反应信息

点击查看最新优质反应信息

文献信息

  • 3-[2,4-(Disubstituted)-phenyl]azacycloalkanones as analgesics
    申请人:Pfizer Inc.
    公开号:US04263438A1
    公开(公告)日:1981-04-21
    Azacycloalkanes, and derivatives thereof, including unsaturated analogs, each of which has at the 3-position a 2-hydroxy-4-substituted phenyl group wherein the 4-position substituent is alkyl which can have an oxygen atom as part of the chain, or aralkyl which can have an oxygen atom as part of the alkyl chain, their use for pharmacological and medicinal purposes, intermediates therefor and processes for their preparation.
    Azacycloalkanes及其衍生物,包括不饱和类似物,每个分子在3位具有一个2-羟基-4-取代苯基基团,其中4位取代基是烷基,可以将氧原子作为链的一部分,或是芳基烷基,可以将氧原子作为烷基链的一部分。这些化合物可用于药理学和医学目的,其中间体以及制备它们的方法。
  • 3-(2-Hydroxy-4-(substituted)phenyl)azacycloalkanes as analgesics
    申请人:Pfizer, Inc.
    公开号:US04332942A1
    公开(公告)日:1982-06-01
    Azacycloalkanes, and derivatives thereof, including unsaturated analogs, each of which has at the 3-position a 2-hydroxy-4-substituted phenyl group wherein the 4-position substituent is alkyl which can have an oxygen atom as part of the chain, or aralkyl which can have an oxygen atom as part of the alkyl chain, their use for pharmacological and medicinal purposes, intermediates therefor and processes for their preparation.
    Azacycloalkanes及其衍生物,包括不饱和类似物,每个分子在3位具有2-羟基-4-取代苯基团,其中4位取代基是烷基,可以在链中具有氧原子,或是芳基烷基,可以在烷基链中具有氧原子,它们用于药理和医学目的,中间体及其制备方法。
  • 9,11-Methano-13-aza-11a-carbathrombanoic acid analogues and pharmaceutical use thereof
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP0044711A1
    公开(公告)日:1982-01-27
    The 9,11-methano-13-aza-11a-carbathrombanoic acid analogues of the general formula: [wherein A represents (i) -CH2CH2-(CH2)m- , (ii) -CH CH-(CH2)m- , (iii) -CH2-O-(CH2)m or (iv) (in which m is an integer of 1 to 6, the double bond between the carbon atoms in positions 5 and 6 in (iv) is in cis or trans-configuration or a mixture thereof and the phenylene group in (iv) represents o-, m- orp-phenylene), R1 represents a hydrogen atom or a straight- or branched-chain alkyl group of 1 to 12 carbon atoms, two R2 both represent hydrogen atoms or methyl groups, R3 represents a hydrogen atom or a hydroxy group, R4 represents a single bond or a straight- or branched-chain alkylene group of 1 to 5 carbon atoms, R5 represents (i) a straight- or branched-chain alkyl, alkoxy or alkylthio group of 1 to 8 carbon atoms, (ii) a cycloalkyl or cycloalkyloxy group of 4 to 7 carbon atoms being unsubstituted or substituted by at least one straight- or branched-chain alkyl group of 1 to 8 carbon atoms or (iii) (in which Z represents a single bond, an oxygen atom or a sulfur atom and R6 may occupy any of the free positions on the phenyl ring and represents a hydrogen atom, a halogen atom, a hydroxy group, a straight- or branched-chain alkyl or alkoxy group of 1 to 5 carbon atoms, a trihalomethyl group, an amino group or a mono- or dialkyl-amino group of 1 to 5 carbon atoms) and the wavy line attached to the carbon atom in position 15 represents a- or β-configuration or a mixture thereof, provided that, when R3 represents a hydroxy group and R4 represents a single bond, R5 does not represent an alkoxy group, an alkylthio group, a cycloalkyloxy group, a phenoxy group and a phenylthio group), and cyclodextrin clathrates thereof, and when R1 represents a hydrogen atom, non-toxic salts thereof, possess strong inhibitory activities on platelet aggregation and on aorta contraction, and are useful for prevention and treatment of diseases which are induced by thromboxane A2.
    通式为 9,11-甲桥-13-氮杂-11a-卡巴曲霉酸类似物: [其中 A 代表 (i) -CH2CH2-(CH2)m- 、 (ii) -CH CH-(CH2)m- 、 (iii) -CH2-O-(CH2)m 或 (iv) (其中 m 为 1 至 6 的整数,(iv)中位于 5 和 6 位的碳原子之间的双键为顺式或反式构型或其混合物,(iv) 中的亚苯基代表邻、间或对亚苯基)、R1 代表氢原子或 1 至 12 个碳原子的直链或支链烷基,两个 R2 均代表氢原子或甲基,R3 代表氢原子或羟基,R4 代表单键或 1 至 5 个碳原子的直链或支链亚烷基,R5 代表 (i) 1 至 8 个碳原子的直链或支链烷基、烷氧基或硫代烷基、 (ii) 未被取代或被至少一个 1 至 8 个碳原子的直链或支链烷基取代的 4 至 7 个碳原子的环烷基或环烷氧基,或 (iii) (其中 Z 代表单键)。 (其中 Z 代表单键、氧原子或硫原子,R6 可占据苯环上的任一自由位置,并代表氢原子、卤素原子、羟基、1 至 5 个碳原子的直链或支链烷基或烷氧基、三卤甲基、当 R3 代表羟基和 R4 代表单键时,R5 不代表烷氧基、烷硫基、环烷氧基、苯氧基和苯硫基)、 及其环糊精包合物,以及当 R1 代表氢原子时,其无毒盐,对血小板聚集和主动脉收缩具有很强的抑制活性,可用于预防和治疗由血栓素 A2 诱导的疾病。
  • US4147872A
    申请人:——
    公开号:US4147872A
    公开(公告)日:1979-04-03
  • US4263438A
    申请人:——
    公开号:US4263438A
    公开(公告)日:1981-04-21
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