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4-甲基伞形酮苯胺肟 | 500024-30-6

中文名称
4-甲基伞形酮苯胺肟
中文别名
——
英文名称
N-hydroxy-4-(methylthio)benzenecarboximidamide
英文别名
4-methylsulfanyl-benzamidoxime;N-hydroxy-4-methylsulfanylbenzamidine;4-Methylsulfanylbenzamide oxime;N'-hydroxy-4-methylsulfanylbenzenecarboximidamide
4-甲基伞形酮苯胺肟化学式
CAS
500024-30-6
化学式
C8H10N2OS
mdl
——
分子量
182.246
InChiKey
FERZLTOGCPKONO-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:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    83.9
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2930909090

SDS

SDS:ae2f454db83704245b1e0c22bbee786e
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反应信息

  • 作为反应物:
    描述:
    4-甲基伞形酮苯胺肟 在 sodium azide 、 三乙胺 作用下, 以 为溶剂, 生成 5-(azidomethyl)-3-(4-(methylthio)phenyl)-1,2,4-oxadiazole
    参考文献:
    名称:
    一些带有1,2,4-恶二唑和1,2,3-三唑部分的氮杂大环的合成
    摘要:
    摘要从1,4开始合成了一个在两个氮原子上带有炔丙基的四氮杂row醚4,9-二(prop-2-yn-1-yl)-1,4,9,12-四氮杂环十六烷-2,11-二酮,9,12-四氮杂环十六烷-2,11-二酮并与通过酰化制备的5-(叠氮甲基)-3-(4-R-苯基)-1,2,4-恶二唑进行1,3-环加成反应。将相应的对位取代的苯甲酰胺肟与氯乙酰氯混合,然后进行叠氮化。以这种方式,成功地获得了一系列带有1,2,4-恶二唑和1,2,3-三唑环的氮杂皇冠醚,并通过光谱/物理数据阐明了它们的结构。
    DOI:
    10.1134/s1070428020040193
  • 作为产物:
    描述:
    对甲硫基苯甲腈羟胺 作用下, 以 乙醇 为溶剂, 生成 4-甲基伞形酮苯胺肟
    参考文献:
    名称:
    可回收王树脂负载磺酸催化剂高效合成2-取代喹唑啉-4(3H)-酮
    摘要:
    摘要::以靛红酸酐为原料,采用可回收的聚合物负载磺酸催化剂,开发了一种高效合成2-取代喹唑啉-4(3H)-酮类化合物的方法。优异的官能团相容性和高产量是该协议的重要特征。
    DOI:
    10.2174/1570178617999201109203731
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文献信息

  • Imidazole hydrochloride promoted synthesis of 3,5-disubstituted-1,2,4-oxadiazoles
    作者:Xuetong Wang、Yin Wang、Xiaoling Liu、Tingshu He、Lingli Li、Huili Wu、Shangjun Zhou、Dan Li、Siwei Liao、Ping Xu、Xing Huang、Jianyong Yuan
    DOI:10.1016/j.tet.2021.132496
    日期:2021.11
    Imidazole hydrochloride as an additive promotes the reaction of amidoximes and DMA derivatives to generated 3,5-disubstituted-1,2,4-oxadiazoles in low to excellent yields without the use of coupling reagents, oxidants, strong acids or bases and other additives.
    咪唑盐酸盐作为添加剂促进酰胺肟和 DMA 衍生物反应生成 3,5-二取代-1,2,4-恶二唑,收率从低到高,无需使用偶联剂、氧化剂、强酸或强碱和其他添加剂。
  • Synthesis of novel triazoles bearing 1,2,4-oxadiazole and phenylsulfonyl groups by 1,3-dipolar cycloaddition of some organic azides and their biological activities
    作者:Yaşar DÜRÜST、Hamza KARAKUŞ、Muhsine Zeynep YAVUZ、Ali Akçahan GEPDİREMEN
    DOI:10.3906/kim-1309-59
    日期:——
    1,3-Dipolar cycloaddition of 5-azidomethyl-3-p-substituted phenyl-1,2,4-oxadiazoles to phenyl vinyl sulfone and bismaleimide gives rise straightforwardly to 1-((3-(p-substituted) phenyl-1,2,4-oxadiazol-5-yl)methyl)-4-(phenylsul\-fonyl)-4,5-dihydro-1H-1,2,3-triazoles and bisdihydropyrrolo[3,4-d][1,2,3]triazole-4,6(3aH,5H)-diones. The structures of the new cycloadducts were elucidated by means of IR, NMR (^1H, ^13}C, 2D), mass spectra, and physical characteristics (mp and R_f values). In addition, anticancer activities of the cycloadducts against MCF-7 cells were also investigated.
    5-叠氮甲基-3-对取代苯基-1,2,4-嗯二唑与苯基乙烯砜和双马来酰亚胺的1,3-偶极环加成反应,直接生成1-((3-(对取代)苯基-1,2,4-嗯二唑-5-基)甲基)-4-(苯磺酰基)-4,5-二氢-1H-1,2,3-三唑和双二氢吡咯并[3,4-d][1,2,3]三唑-4,6(3aH,5H)-二酮。通过红外、核磁共振(^1H、^13C、2D)、质谱和物理性质(熔点和R_f值)阐明了新环加合物的结构。此外,还研究了这些环加合物对MCF-7细胞的抗癌活性。
  • An Efficient Synthesis of 2-Substituted Quinazolin-4(3H)-ones Catalyzed by Iron(III) Chloride
    作者:Jayaprakash Sarva、Ramamohan Mekala、Raghunadh Akula、Raghavendra Kamaraju、Chandrasekhar Bannoth、Sridhar Regati
    DOI:10.1055/s-0033-1340786
    日期:——
    A simple and highly efficient synthesis of 2-substituted quinazolin-4(3 H )-ones by the iron(III) chloride catalyzed reaction of isatoic anhydride with various amidoxime derivatives was developed. Several aryl and alkyl amidoximes were screened to demonstrate the scope of the methodology.
    开发了一种简单高效的 2-取代喹唑啉-4(3 H)-酮的合成方法,通过氯化铁 (III) 催化的靛红酸酐与各种胺肟衍生物的反应。筛选了几种芳基和烷基酰胺肟以证明该方法的范围。
  • NH-acidities and Hammett correlation of 3-para substituted phenyl-1,2,4-oxadiazol-5(4$H)$-ones and 1,2 $\lambda^{4}$3,5-oxathiadiazole 2-oxides in nonaqueous media
    作者:Nedime DÜRÜST、Yaşar DÜRÜST、Emine Özge GÖZLÜKAYA
    DOI:10.3906/kim-1303-46
    日期:——
    NH acidities of some 3-(p-substitutedphenyl)-1,2,4-oxadiazol-5(4H)-ones and 4-(p-substitutedphenyl)-1,2 \lambda^43,5-oxathiadiazole 2-oxides were determined in methanol by means of potentiometric titration with sodium methoxide. pK_a values of the title compounds calculated from the potentiometric data were interpreted on the basis of structural effects caused by para-substituted groups on the phenyl ring by plotting pK_a values versus Hammett \sigma_p^+ constants, which gave excellent linear correlations.
    一些3-(对取代苯基)-1,2,4-噁二唑-5(4H)-酮和4-(对取代苯基)-1,2λ^43,5-噻二氮杂烯-2-氧化物的NH酸度在甲醇中通过与甲氧化钠的电位滴定进行测定。根据电位数据计算出的标题化合物的pK_a值通过绘制pK_a值与Hammett σ_p^+常数的关系图来解释,这表明对取代基对苯环造成的结构效应,得到了很好的线性相关性。
  • [EN] FUNGICIDAL OXADIAZOLES<br/>[FR] OXADIAZOLES FONGICIDES
    申请人:DU PONT
    公开号:WO2018080859A1
    公开(公告)日:2018-05-03
    Disclosed are compounds of Formula I, including all geometric and stereoisomers, tautomers, N-oxides, and salts thereof, wherein R1, Z1, R2, Z2, J, s and f are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula I and methods for controlling plant disease caused by a fungal pathogen comprising applying an effective amount of a compound or a composition of the invention.
    揭示了公式I的化合物,包括所有几何和立体异构体、互变异构体、N-氧化物和盐,其中R1、Z1、R2、Z2、J、s和f的定义如披露所述。还揭示了含有公式I化合物的组合物,以及用于控制由真菌病原体引起的植物疾病的方法,包括施用本发明的化合物或组合物的有效量。
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