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(R)-tert-Butyl(4-hydroxybutan-2-yl)carbamic acid

中文名称
——
中文别名
——
英文名称
(R)-tert-Butyl(4-hydroxybutan-2-yl)carbamic acid
英文别名
tert-butyl-[(2R)-4-hydroxybutan-2-yl]carbamic acid
(R)-tert-Butyl(4-hydroxybutan-2-yl)carbamic acid化学式
CAS
——
化学式
C9H19NO3
mdl
——
分子量
189.25
InChiKey
WQXRMDAHTONQSR-SSDOTTSWSA-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):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    60.8
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • MOLECULES HAVING PESTICIDAL UTILITY, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES, RELATED THERETO
    申请人:Dow AgroSciences LLC
    公开号:US20170210723A1
    公开(公告)日:2017-07-27
    This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, compositions containing such molecules, and processes of using such molecules and compositions against such pests. These molecules and compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).
    这份披露涉及具有对节肢动物门、软体动物门和线虫门害虫具有杀虫效用的分子领域,用于生产这种分子的过程,用于这种过程的中间体,含有这种分子的组合物,以及使用这种分子和组合物对抗这些害虫的过程。这些分子和组合物可以用作杀螨剂、杀虫剂、杀螨剂、杀软体动物剂和杀线虫剂。本文件披露了具有以下式(“式一”)的分子。
  • Metallo-beta-lactamase inhibitors
    申请人:Merck Sharp & Dohme Corp.
    公开号:US10544130B2
    公开(公告)日:2020-01-28
    The present invention relates to metallo-β-lactamase inhibitor compounds of Formula I: and pharmaceutically acceptable salts thereof, wherein Z, RA, X1, X2 and R1 are as defined herein. The present invention also relates to compositions which comprise a metallo-β-lactamase inhibitor compound of the invention or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, optionally in combination with a beta lactam antibiotic and/or a beta-lactamase inhibitor. The invention further relates to methods for treating a bacterial infection comprising administering to a patient a therapeutically effective amount of a compound of the invention, in combination with a therapeutically effective amount of one or more β-lactam antibiotics and optionally in combination with one or more beta-lactamase inhibitor compounds. The compounds of the invention are useful in the methods described herein for overcoming antibiotic resistance.
    本发明涉及式 I 的金属-β-内酰胺酶抑制剂化合物: 及其药学上可接受的盐,其中Z、RA、X1、X2和R1如本文所定义。本发明还涉及组合物,该组合物包含本发明的金属-β-内酰胺酶抑制剂化合物或其药学上可接受的盐,以及药学上可接受的载体,可选择与β-内酰胺抗生素和/或β-内酰胺酶抑制剂结合使用。本发明进一步涉及治疗细菌感染的方法,包括向患者施用治疗有效量的本发明化合物,与治疗有效量的一种或多种β-内酰胺类抗生素联合使用,也可选择与一种或多种β-内酰胺酶抑制剂化合物联合使用。本发明的化合物在本文所述的克服抗生素耐药性的方法中是有用的。
  • METALLO-BETA-LACTAMASE INHIBITORS
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20190144432A1
    公开(公告)日:2019-05-16
    The present invention relates to metallo-β-lactamase inhibitor compounds of Formula I: and pharmaceutically acceptable salts thereof, wherein Z, R A , X 1 , X 2 and R 1 are as defined herein. The present invention also relates to compositions which comprise a metallo-β-lactamase inhibitor compound of the invention or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, optionally in combination with a beta lactam antibiotic and/or a beta-lactamase inhibitor. The invention further relates to methods for treating a bacterial infection comprising administering to a patient a therapeutically effective amount of a compound of the invention, in combination with a therapeutically effective amount of one or more β-lactam antibiotics and optionally in combination with one or more beta-lactamase inhibitor compounds. The compounds of the invention are useful in the methods described herein for overcoming antibiotic resistance.
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