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N-Benzoyl-thiobenzamid | 4194-36-9

中文名称
——
中文别名
——
英文名称
N-Benzoyl-thiobenzamid
英文别名
N-Thiobenzoyl-benzamid;Benzamide,n-(phenylthioxomethyl)-;N-(benzenecarbonothioyl)benzamide
N-Benzoyl-thiobenzamid化学式
CAS
4194-36-9
化学式
C14H11NOS
mdl
——
分子量
241.313
InChiKey
HVDGFNULWROUNW-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:
    119 °C
  • 密度:
    1.28 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    61.2
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2930909090

SDS

SDS:3d65f614dbc414ccd6abfa936bee8eb5
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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

  • 作为反应物:
    参考文献:
    名称:
    Deshpande,P.H., Journal of the Indian Chemical Society, 1969, vol. 46, p. 1096 - 1101
    摘要:
    DOI:
  • 作为产物:
    描述:
    N-硫代苯甲酰苯甲脒 生成 N-Benzoyl-thiobenzamid
    参考文献:
    名称:
    Kresze,G. et al., Chemische Berichte, 1965, vol. 98, p. 3401 - 3409
    摘要:
    DOI:
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文献信息

  • The triethylamine catalyzed reaction of N,N-disubstituted thioamide–bromine adducts with unsubstituted thiobenzamide
    作者:Antonino Corsaro、Anna Compagnini、Giancarlo Perrini、Giovanni Purrello
    DOI:10.1039/p19840000897
    日期:——
    The reaction of N,N-disubstituted thioamide–bromine adducts with unsubstituted thioamide, followed by treatment with triethylamine, affords novel N′-thiobenzoylamidines along with smaller amounts of secondary products. A mechanism is proposed for the formation of the amidines. The results give an insight into the initial steps of the mechanism by which thioamides are converted into 1,2,4-thiadiazoles
    的反应Ñ,Ñ二取代的硫代酰胺-溴加成物与未取代的硫代酰胺,随后用三乙胺处理,得到新颖Ñ '与较少量的副产物的沿-thiobenzoylamidines。提出了形成the的机制。结果使人们深入了解了将硫酰胺转化为1,2,4-噻二唑的机理的初始步骤。
  • THERAPEUTIC COMBINATIONS
    申请人:SUPERSALUS, INC.
    公开号:US20200253926A1
    公开(公告)日:2020-08-13
    Methods of treatment include administering effective amounts of a nitrogen oxide (NO) donor (such as nicorandil) and a hydrogen sulfide (H 2 S) releasing agent (such as zofenopril) to a subject in need thereof. In various embodiments, the H 2 S releasing agent is administered in an amount that is effective to enhance the therapeutic efficacy of the NO donor. Coformulations of the H 2 S releasing agent and the NO donor are provided that are suitable for treating a number of conditions. In various embodiments, treatments for conditions such as chronic kidney disease, Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, familial dilated cardiomyopathy and/or idiopathic dilated cardiomyopathy are provided.
    治疗方法包括向需要的对象施用有效量的一氧化氮(NO)供体(如尼可拉地尔)和硫化氢(H2S)释放剂(如左非诺普利)。在各种实施方式中,以有效量施用H2S释放剂以增强NO供体的治疗功效。提供了H2S释放剂和NO供体的联合制剂,适用于治疗多种疾病。在各种实施方式中,提供了治疗慢性肾病、杜兴氏肌肉萎缩症、贝克氏肌肉萎缩症、家族性扩张型心肌病和/或特发性扩张型心肌病等疾病的方法。
  • Non-toxic corrosion-protection pigments based on manganese
    申请人:——
    公开号:US20040011252A1
    公开(公告)日:2004-01-22
    Corrosion-inhibiting pigments based on manganese are described that contain a trivalent or tetravalent manganese/valence stabilizer complex. An inorganic or organic material is used to stabilize the trivalent or tetravalent manganese ion to form a compound that is sparingly soluble, exhibits low solubility, or is insoluble in water, depending upon the intended usage. Specific stabilizers are chosen to control the release rate of trivalent or tetravalent manganese during exposure to water and to tailor the compatibility of the powder when used as a pigment in a chosen binder system. Stabilizers may also modify the processing and handling characteristics of the formed powders. Manganese/valence stabilizer combinations are chosen based on the well-founded principles of manganese coordination chemistry. Many manganese-valence stabilizer combinations are presented that can equal the performance of conventional hexavalent chromium or tetravalent lead systems. It is emphasized that this abstract is provided to comply with the rules requiring an abstract which will allow a searcher or other reader to quickly ascertain the subject matter of the technical disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims.
    以锰为基础的缓蚀颜料含有三价或四价锰/价稳定剂复合物。一种无机或有机材料可用于稳定三价或四价锰离子,从而形成一种可少量溶解、溶解度低或不溶于水的化合物,具体取决于预期用途。选择特定的稳定剂是为了控制三价锰或四价锰在遇水时的释放率,并调整粉末在所选粘合剂体系中用作颜料时的相容性。稳定剂还可以改变成型粉末的加工和处理特性。锰/价稳定剂组合的选择是基于锰配位化学的基本原理。文中介绍了许多锰价稳定剂组合,其性能与传统的六价铬或四价铅体系相当。需要强调的是,提供本摘要是为了符合要求提供摘要的规则,以便检索者或其他读者快速确定技术公开的主题。提交本摘要的前提是,本摘要不用于解释或限制权利要求的范围或含义。
  • Non-toxic corrosion-protection pigments based on rare earth elements
    申请人:——
    公开号:US20040104377A1
    公开(公告)日:2004-06-03
    A corrosion-inhibiting pigment comprising a rare earth element and a valence stabilizer combinded to form a rare earth/valence stabilizer complex. The rare earth element is selected from cerium, terbium, praseodymium, or a combination thereof, and at least one rare earth element is in the tetravalent oxidation state. An inorganic or organic material is used to stabilize the tetravalent rare earth ion to form a compound that is sparingly soluble in water. Specific stabilizers are chosen to control the release rate of tetravalent cerium, terbium, or praseodymium during exposure to water and to tailor the compatibility of the powder when used as a pigment in a chosen binder system. Stabilizers may also modify the processing and handling characteristics of the formed powders. Many rare earth-valence stabilizer combinations are presented that can equal the performance of conventional hexavalent chromium systems.
    一种缓蚀颜料,由稀土元素和价态稳定剂结合形成稀土/价态稳定剂复合物。稀土元素选自铈、铽、镨或它们的组合,至少有一种稀土元素处于四价氧化态。使用无机或有机材料来稳定四价稀土离子,以形成稀溶于水的化合物。选择特定的稳定剂是为了控制四价铈、铽或镨在遇水时的释放率,并调整粉末在所选粘合剂体系中用作颜料时的相容性。稳定剂还可以改变成型粉末的加工和处理特性。本文介绍了许多稀土-价稳定剂组合,其性能可与传统的六价铬体系媲美。
  • Domino Aryne Precursor: Efficient Construction of 2,4-Disubstituted Benzothiazoles
    作者:Jiarong Shi、Dachuan Qiu、Juan Wang、Hai Xu、Yang Li
    DOI:10.1021/jacs.5b02566
    日期:2015.5.6
    An aryne precursor with a potential to perform domino aryne chemistry was proposed and synthesized. The reaction of this reagent with benzothioamide derivatives could afford 2,4-disubstituted benzothiazole with sequential incorporation of C-S, C-N, and C-C bonds on the consecutive three positions of the aryne precursor.
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