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2-phenethyl-succinic acid 4-tert-butyl ester 1-methyl ester | 92828-42-7

中文名称
——
中文别名
——
英文名称
2-phenethyl-succinic acid 4-tert-butyl ester 1-methyl ester
英文别名
4-O-tert-butyl 1-O-methyl 2-(2-phenylethyl)butanedioate
2-phenethyl-succinic acid 4-tert-butyl ester 1-methyl ester化学式
CAS
92828-42-7
化学式
C17H24O4
mdl
——
分子量
292.375
InChiKey
ZJMXJIYXMQWVLQ-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):
    3.2
  • 重原子数:
    21
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 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

  • Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex
    申请人:Gravel Denis
    公开号:US20060135480A1
    公开(公告)日:2006-06-22
    The present invention relates to derivatives of succinic and glutaric acids and analogues thereof, having the following general formula (I), useful as inhibitors of PHEX. These derivatives are useful for promoting generation of bone mass and treating or preventing diseases or conditions associated with a phosphate metabolism defect. Methods for preparation and intermediates are also disclosed.
    本发明涉及琥珀酸和戊二酸的衍生物及其类似物,具有以下一般式(I),可用作PHEX的抑制剂。这些衍生物有助于促进骨量的生成,并治疗或预防与磷酸盐代谢缺陷相关的疾病或病症。本发明还公开了制备方法和中间体。
  • Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of PHEX
    申请人:Gravel Denis
    公开号:US20060287280A1
    公开(公告)日:2006-12-21
    The present invention relates to derivatives of succinic and glutaric acids and analogues thereof, having the following general formula: useful as inhibitors of PHEX. These derivatives are useful for promoting generation of bone mass and treating or preventing diseases or conditions associated with a phosphate metabolism defect. Methods for preparation and intermediates are also disclosed.
    本发明涉及琥珀酸和戊二酸及其类似物的衍生物,其具有以下一般式:用作PHEX的抑制剂。这些衍生物有助于促进骨量的生成,并用于治疗或预防与磷酸盐代谢缺陷有关的疾病或病况。本发明还公开了制备方法和中间体。
  • Method of preparing optically active homo-beta-amino acids
    申请人:MONSANTO COMPANY
    公开号:EP0561758A2
    公开(公告)日:1993-09-22
    The present invention is directed to synthesis of homo-β-amino acids of an optical purity sufficient to exhibit optical activity wherein Curtius rearrangement of 3-mono-substituted succinate acid half ester of an optical purity sufficient to exhibit optical activity is affected and the incipient isocyanate is trapped with a primary or secondary alcohol. The resulting carbamate-protected homo-β-amino esters are then saponified to produce the corresponding carbamate-protected homo-β-amino acids which are deprotected to yield homo-β-amino acids of an optical purity sufficient to exhibit optical activity.
    本发明旨在合成光学纯度足以显示光学活性的均-β-氨基酸,其中光学纯度足以显示光学活性的3-单取代琥珀酸半酯的Curtius重排受到影响,而初生异氰酸酯被伯醇或仲醇截留。得到的氨基甲酸酯保护的均-β-氨基酯然后进行皂化,生成相应的氨基甲酸酯保护的均-β-氨基酸,再进行脱保护,生成光学纯度足以显示光学活性的均-β-氨基酸。
  • DERIVATIVES OF SUCCINIC AND GLUTARIC ACIDS AND ANALOGS THEREOF USEFUL AS INHIBITORS OF PHEX
    申请人:Enobia Pharma Inc.
    公开号:EP1572645A2
    公开(公告)日:2005-09-14
  • US7105539B2
    申请人:——
    公开号:US7105539B2
    公开(公告)日:2006-09-12
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