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Hexanothiohydroxamic Acid | 132637-58-2

中文名称
——
中文别名
——
英文名称
Hexanothiohydroxamic Acid
英文别名
N-hydroxyhexanethioamide
Hexanothiohydroxamic Acid化学式
CAS
132637-58-2
化学式
C6H13NOS
mdl
——
分子量
147.241
InChiKey
NUVGQZKUHNKMEH-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):
    1.6
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    64.4
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-硝基己烷双(三甲基硫化硅) 、 potassium hydride 作用下, 生成 Hexanothiohydroxamic Acid
    参考文献:
    名称:
    Counterattack reagents: Thiosilanes in the conversion of nitro compounds to thiohydroxamic acids and thiohydroximates
    摘要:
    DOI:
    10.1016/s0040-4020(01)89057-8
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文献信息

  • EP1461324A4
    申请人:——
    公开号:EP1461324A4
    公开(公告)日:2006-02-01
  • HETEROCYCLIC COMPOUNDS, COMBINATORIAL LIBRARIES THEREOF AND METHODS OF SELECTING DRUG LEADS
    申请人:Yissum Research Development Company of the Hebrew University of Jerusalem
    公开号:EP1461324A2
    公开(公告)日:2004-09-29
  • [EN] HETEROCYCLIC COMPOUNDS, COMBINATORIAL LIBRARIES THEREOF AND METHODS OF SELECTING DRUG LEADS<br/>[FR] COMPOSES HETEROCYCLIQUES, BANQUES COMBINATOIRES DE CEUX-CI ET PROCEDES DE SELECTION DE MEDICAMENTS TETES DE SERIE
    申请人:YISSUM RES DEV CO
    公开号:WO2003059876A2
    公开(公告)日:2003-07-24
    The present invention provides new heterocyclic compounds that have a relatively flexible backbone. These compounds may be used to produce new combinatorial libraries that will permit screening for lead compounds and selection of drug candidates for a variety of uses in human medicine, veterinary medicine and in agriculture. The members of libraries provided by the invention differ from each other (in addition to the conventional chemical and positional diversity attained by the different substituents on the ring) in two novel aspects : (a) the ring size; and (b) the chirality of the substituents on the ring. This leads to conformational diversity and flexibility that allows the selection of the most active compound, not only on the basis of the nature and proper arrangement of the substituents attained by the known chemical and positional diversity, but also based on the ability to undergo conformational complementarity attained by the conformational diversity. The present invention further provides combinatorial libraries comprising a plurality of the heterocyclic compounds of the present invention, and methods of screening the combinatorial libraries for compounds having a beneficial biological effect. The screening methods provided herein may be automated and/or computerized, for example by using a computer program to virtually screen the combinatorial libraries in order to identify compounds that are predicted to adopt bioactive conformations that will give rise to the desired biological effect.
  • Counterattack reagents: Thiosilanes in the conversion of nitro compounds to thiohydroxamic acids and thiohydroximates
    作者:Jih Ru Hwu、Shwu-Chen Tsay
    DOI:10.1016/s0040-4020(01)89057-8
    日期:——
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同类化合物

镉离子通道 I 铅离子载体III 硫代乙酰胺 硫代丙酰胺乙酯 硫代丙酰胺 环戊烷羟基硫胺 环丙烷硫代甲酰胺 环丁烷羟基硫胺 氰酸根硫杂酰胺,二-2-丙烯基-(9CI) 戊硫酸三甲基硅烷基甲基-酰胺 己硫代酰胺 双十二烷基二硫代乙二酰胺 二硫代乙酰胺 二甲胺基硫代乙酰胺盐酸盐 [2H9]-2,2-二甲基硫代丙酰胺 S-[5-(二甲基氨基)-5-硫代戊基]硫代乙酸酯 N-甲基乙烷二(硫代酰胺) N-乙基硫代乙酰胺 N-(乙氧基羰基)硫代丙酰胺 N-(2-甲氧基乙基)-N-甲基硫代丙酰胺 N-(2-氨基-2-硫代乙基)乙酰胺 N,N-二甲基硫代乙酰胺 N,N-二甲基癸烷硫代酰胺 N,N-二甲基-10-十一碳烯硫代酰胺 N,N-二异丙基硫代丙酰胺 N,N-二异丙基乙烷硫代酰胺 N,N-二乙基丁烷硫代酰胺 N,N-二乙基-3-甲基硫代丁酰胺 N,N-二乙基-2-甲基硫代丙酰胺 N,N-二乙基-2-(三甲基硅烷基)硫代乙酰胺 N,N-二乙基-2,2-二甲基丙烷硫代酰胺 N,N-二丙基-硫代丙酰胺 N,N-二丁基丁烷硫代酰胺 N,N,N',N'-四乙基二硫代草酰胺 N,N,N',N'-四(十二烷基)乙烷二硫代酰胺 N,N,3,3-四甲基硫代丁酰胺 N,N'-二甲基二硫代乙酰胺 N,N'-二环己基-二硫代乙酰胺 N,N'-二戊基乙烷二硫代酰胺 N,N'-二己基二硫代乙酰胺 N,N'-二丙基乙烷二硫代酰胺 N,N'-二[3-(二甲基氨基)丙基]二硫代草酰胺 N,N'-二(十八烷基)乙烷二硫代酰胺 N,N'-二(仲-丁基)乙烷二硫代酰胺 N,N'-二(3-甲氧基丙基)二硫代乙酰胺 N,N'-二(2-羟基乙基)二硫代乙酰胺 N,N'-二(2-羟基丙基)二硫代乙酰胺 N,N'-二(2-甲氧基乙基)乙烷二硫代酰胺 N,N'-二(2-二甲基氨基乙基)乙烷二硫代酰胺 4-噻唑乙酸乙酯