摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

diethyl(imino)-λ4-sulfane sulfate | 24507-57-1

中文名称
——
中文别名
——
英文名称
diethyl(imino)-λ4-sulfane sulfate
英文别名
S,S-diethyl-sulfimide;S,S-diethyl-sulfimine;S,S-Diaethyl-sulfimin;Diaethylsulfilimin;Diethylsulfilimin;Diaethylsulfimin;Diethyl(imino)-lambda4-sulfane;diethyl(imino)-λ4-sulfane
diethyl(imino)-λ4-sulfane sulfate化学式
CAS
24507-57-1
化学式
C4H11NS
mdl
——
分子量
105.204
InChiKey
DDZCXIAMYYJPDL-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:
    -12--11 °C
  • 沸点:
    147.7±23.0 °C(Predicted)
  • 密度:
    1.01±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    6
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    43.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    diethyl(imino)-λ4-sulfane sulfate亚硝酰氯 作用下, 生成 Diaethylsulfodistickstoffmonoxid
    参考文献:
    名称:
    MacCordick,J.; Appel,R., Zeitschrift fur Naturforschung. Teil B: Chemie, Biochemie, Biophysik, Biologie, 1969, vol. 24, p. 938
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    N-未取代的硫亚胺的合成及某些性质
    摘要:
    多种S-aminosulfonium mesitylenesulfonates的,R 1 - [R 2小号+ NH 2 ·X - ,分别以高收率由硫化物用O- mesitylenesulfonylhydroxylamine(MSH)的反应来制备。检查了衍生的亚硫亚胺的热稳定性。烯丙基硫化物与MSH的反应直接提供了烯丙基胺的盐,收率很高,大概是通过可溶的烯丙基硫亚胺的[2,3]-σ重排,然后是SN键断裂。还描述了二硫化物和硫酮与MSH的反应。
    DOI:
    10.1016/0040-4020(75)80143-8
点击查看最新优质反应信息

文献信息

  • [EN] ANTHRANILAMIDE COMPOUNDS AND THEIR USE AS PESTICIDES<br/>[FR] COMPOSÉS D'ANTHRANILAMIDE ET LEUR UTILISATION COMME PESTICIDES
    申请人:BASF SE
    公开号:WO2015028501A1
    公开(公告)日:2015-03-05
    The present invention relates to anthranilamide compounds of the formula I and the stereoisomers, salts, tautomers and N-oxides thereof and to compositions comprising the same. The invention also relates to the use of the anthranilamide compounds or of the compositions comprising such compounds for combating invertebrate pests. Furthermore, the invention relates to methods of applying such compounds. Wherein k is 0, 1, 2 or 3; Q is N or CH; R1 is inter alia hydrogen, halogen, SF5, -SCN, nitro, azido, C1-C8-alkyl, C1-C8-haloalkyl etc., R2 is inter alia selected from hydrogen, C1-C6 alkyl etc.; R3 is selected from the group consisting of hydrogen, halogen, cyano, azido, nitro, -SCN, SF5, C1-C6-alkyl which may be partially or fully halogenated etc.; R4 is hydrogen, halogen or C1-C4-haloalkyl; R5 is a radical R5-a or R5-b where p is 0 or 1; and where R5a and R5b are as defined in the claims: R6 is selected from the group consisting of C1-C6 alkyl, C1-C6 haloalkyl, C1-C4-alkoxy- C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkyl, etc; Y is N or C-R7, where R7 is as defined in the claims; Z is CN or a moiety of the formula Z1, where X1 is O, S, N-R9, N-O-R9 or N-S-R9; X2 is O, S or NR10, or X2-R8 is a radical of the formulae X-a or X-b as defined in the claims; where R8, R9 and R10 are as defined in the claims.
    本发明涉及公式I的酰胺化合物及其立体异构体、盐、互变异构体和N-氧化物,以及包含这些化合物的组合物。本发明还涉及使用酰胺化合物或包含这些化合物的组合物来对抗无脊椎动物害虫。此外,本发明还涉及应用这些化合物的方法。其中k为0、1、2或3;Q为N或CH;R1包括氢、卤素、SF5、-SCN、硝基、偶氮基、C1-C8-烷基、C1-C8-卤代烷基等;R2包括氢、C1-C6烷基等;R3选自氢、卤素、基、偶氮基、硝基、-SCN、SF5、部分或完全卤代的C1-C6-烷基等;R4为氢、卤素或C1-C4-卤代烷基;R5为基团R5-a或R5-b,其中p为0或1;R5a和R5b的定义如索赔中所述;R6选自C1-C6烷基、C1-C6卤代烷基、C1-C4-烷氧基-C1-C4-烷基、C1-C4-卤代烷氧基-C1-C4-烷基等;Y为N或C-R7,其中R7的定义如索赔中所述;Z为CN或具有Z1的基团,其中X1为O、S、N-R9、N-O-R9或N-S-R9;X2为O、S或NR10,或X2-R8为公式X-a或X-b的基团,其中R8、R9和R10的定义如索赔中所述。
  • Substituted mesoionic compounds for combating animal pests
    申请人:BASF SE
    公开号:EP2684879A1
    公开(公告)日:2014-01-15
    A substituted mesoionic compound of formula (I), wherein the symbols have the meanings as given in the description, is useful for combating animal pests.
    公式(I)的取代中间离子化合物,在符号所给出的含义下,对于防治动物害虫是有用的。
  • Free sulfilimines. 5. Preparation and physical and chemical properties of "free" sulfilimines
    作者:Toshiaki Yoshimura、Tetsuo Omata、Naomichi Furukawa、Shigeru Oae
    DOI:10.1021/jo00872a013
    日期:1976.5
  • Appel,R.; Buechner,W., Chemische Berichte, 1962, vol. 95, p. 855 - 866
    作者:Appel,R.、Buechner,W.
    DOI:——
    日期:——
  • Appel et al., Justus Liebigs Annalen der Chemie, 1958, vol. 618, p. 53,58
    作者:Appel et al.
    DOI:——
    日期:——
查看更多

同类化合物

S,S-diisopropyl-sulfimide N-tert-butyloxycarbonyl isopropyl methyl sulfimine N-trifluoroacetyl-methyl isopropylsulfilimine S,S-dipropyl-sulfimide thioaceramide S,S-bis-(2-hydroxy-ethyl)-sulfimide (Dimethyl-lambda4-sulfanylidene)urea N-Acetyliminodiethylsulfuran N-Monochloracetyl-S,S-dimethylsulfimid N-acetyl-S-methyl-S-(perfluorooctyl)sulfilimine Dimethylsulfimin prop-2-enyl N-[2-methoxyethyl(methyl)-lambda4-sulfanylidene]carbamate N-dichloroacetyl-S,S-diethylsulphilimine (4-Aminobutylsulfinimidoyl)formic acid 2-Methyl-1-sulfanylideneguanidine 2-thionitroso-1,4-dihydropyrazine 4-thionitroso-3,4-dihydro-2H-pyran 1-(1-Thionitrosopropyl)cyclohexa-1,3-diene 1-sulfanylidene-2H-pyrazin-1-ium (2-Aminoethylsulfinimidoyl)methanethial 3,6-Dimethylheptyl-imino-methyl-lambda4-sulfane Dimethyl-(2,3,5-trimethylcyclohepta-1,3,6-trien-1-yl)imino-lambda4-sulfane N'-carbamimidoyl-N-sulfanylidenemethanimidamide 2-Dodecyl-1-sulfanylideneguanidine ethane;2-thionitrosoethenamine Sulfanylidene(12-thionitrosododecylimino)-lambda4-sulfane Imino-(2-methylpropyl)-propan-2-yl-lambda4-sulfane Imino(dipentyl)-lambda4-sulfane Cyclopropyl-imino-propan-2-yl-lambda4-sulfane Imino-propan-2-yl-propyl-lambda4-sulfane Cyclobutyl-imino-propan-2-yl-lambda4-sulfane tert-butyl (NE)-N-[methyl(propan-2-yl)-lambda4-sulfanylidene]carbamate N-(dimethyl-lambda4-sulfanylidene)-2,2,2-trifluoroacetamide S-cyclohexyl-S-methyl-N-(trifluoroacetyl)sulfilimine N-acetyl dimethylsulfimide diethyl(imino)-λ4-sulfane sulfate 1-Methylsulfanyl-3-thionitrosopropane