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

5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxamide | 13584-27-5

中文名称
——
中文别名
——
英文名称
5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxamide
英文别名
5,6-dihydro-2-methyl-1,4-oxathiine-3-amide;2-Methyl-5,6-dihydro-1,4-oxathiin-3-carboxamide;6-methyl-2,3-dihydro-1,4-oxathiine-5-carboxamide
5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxamide化学式
CAS
13584-27-5
化学式
C6H9NO2S
mdl
——
分子量
159.209
InChiKey
ODQRPTODALTOCU-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):
    -0.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    77.6
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

SDS

SDS:5054b52ec161e76511e96a82ca8635e9
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Substituent and Solvent Effects on the Photosensitized Oxygenation of 5,6-Dihydro-1,4-oxathiins. Intramolecular Oxygen Transfer vs Normal Cleavage of the Dioxetane Intermediates
    作者:F. Cermola、M. R. Iesce
    DOI:10.1021/jo020008m
    日期:2002.7.1
    ketosulfoxides 7 and 8 depending on the nature of the substituent at C3 and on the reaction conditions. The normal fragmentation of dioxetanes 2 to 4 competes with an intramolecular oxygen transfer to ring sulfur, which leads to 7 and 8, presumably via the labile epoxides 5. This new pathway is promoted by electron-withdrawing groups at C3 and, for unsubstituted and monosubstituted amide derivatives 1h and 1i
    单线态氧与各种取代的氧杂环丁烷1的反应产生二羰基化合物4和/或酮亚砜7和8,这取决于C 3上取代基的性质和反应条件。二氧环乙烷2到4的正常断裂与分子内的氧转移竞争成环硫,这大概是通过不稳定的环氧化物5导致的7和8。这种新的途径是由C3上的吸电子基团促进的,对于未取代的和单取代的酰胺衍生物1h和1i分别通过溶剂呈碱性。化学实验支持7为环氧化物5的中间体,而对于8为环氧化物的结论并不明确。但是,后者的形成似乎受到极性溶剂和C2上的阳离子稳定基团(如苯基或甲基)的帮助。
  • Process for preparing 5,6-dihydro-2-methyl-1,4-oxathiin derivatives
    申请人:——
    公开号:US04152334A1
    公开(公告)日:1979-05-01
    5,6-Dihydro-2-methyl-1,4-oxathiin derivatives are prepared by converting an appropriate 1,3-oxathiolane derivative to its sulfoxide and subjecting the sulfoxide to acid catalyzed rearrangement to form the desired product.
    通过将适当的1,3-噁硫烷衍生物转化为其亚砜并将亚砜受酸催化重排,制备5,6-二氢-2-甲基-1,4-噁硫烷衍生物。
  • Oxathiin carboxamide
    申请人:Dunkel Ralf
    公开号:US20070004793A1
    公开(公告)日:2007-01-04
    This invention relates to novel oxathiincarboxamides of the formula (I) in which G 1 , G 2 , G 3 , n, R 1 , R 2 , R 3 , R 4 , R 5 and Z are as defined in the disclosure, to a plurality of processes for preparing these compounds and their use for controlling unwanted microorganisms, and to novel intermediates and their preparation.
    本发明涉及公式(I)的新颖的噁嗪羧酰胺化合物,其中G1、G2、G3、n、R1、R2、R3、R4、R5和Z如披露中所定义,以及制备这些化合物的多种方法和它们用于控制不良微生物的用途,还涉及新的中间体及其制备。
  • Pesticidal mixtures comprising an anthranilamide insecticide and a fungicide
    申请人:BASF SE
    公开号:EP2489266A2
    公开(公告)日:2012-08-22
    Ternary pesticidal mixtures comprising, as active components, an anthranilamide compound of the formula I which is selected from 3-bromo-4'-cyano-1-(3-chloro-2-pyridyl)-2'-methyl-6'-(methylcarb¬amoyl)pyra¬zole-5-carboxanilide, and 3-bromo-4'-chloro-1-(3-chloro-2-pyridyl)-2'-methyl-6'-(methylcarb¬amoyl)pyrazole-5-carboxanilide; and one fungicidal compound II selected from the group of strobilurins, and one fungicidal compound III selected from the group of azoles; in a synergistically effective amount, methods for controlling pests, and harmful fungi, methods of protecting plants from attack or infestation by insects, acarids or nematodes, methods for treating, controlling, preventing or protecting an animal against infestation or infection by parasites, compositions containing these mixtures, and methods for their preparation.
    三元杀虫混合物,其活性成分包括 式 I 的蒽酰胺化合物 选自 3-溴-4'-氰基-1-(3-氯-2-吡啶基)-2'-甲基-6'-(甲基氨基甲酰基)吡唑-5-甲酰苯胺,和 3-溴-4'-氯-1-(3-氯-2-吡啶基)-2'-甲基-6'-(甲基氨基甲酰基)吡唑-5-甲酰苯胺; 和 一种选自strobilurins类的杀真菌化合物II,和 一种选自唑类的杀真菌化合物 III; 以增效有效的量,控制害虫和有害真菌的方法,保护植物免受昆虫、刺吸虫或线虫攻击或侵扰的方法,治疗、控制、预防或保护动物免受寄生虫侵扰或感染的方法,含有这些混合物的组合物及其制备方法。
  • Eccles, Peter J.; Hudson, Harry R.; Mavrommatis, Christakis N., Phosphorus, Sulfur and Silicon and the Related Elements, 1995, vol. 105, # 1-4, p. 33 - 44
    作者:Eccles, Peter J.、Hudson, Harry R.、Mavrommatis, Christakis N.、Pianka, Max
    DOI:——
    日期:——
查看更多

同类化合物

6-乙氧基-2-甲基-5,6-二氢-1,4-氧硫杂环己二烯-3-羧酸 5,6-二氢-1,4-氧硫杂环己二烯-2-羧酸 5,6,7,8-四氢-4,7-二甲基-1,2-苯并氧硫杂环己二烯 2,2-二氧化物 2-甲基-5,6-二氢-1,4-氧硫杂环己二烯-3-甲酸 2-甲基-1,4-氧硫杂环己二烯-3-羧酸 1-(6-乙氧基-2-甲基-4-氧代-5,6-二氢-1,4-氧硫杂环己二烯-3-基)乙酮 1,4-苯并氧硫杂环己二烯4,4-二氧化物 1,4-氧硫杂环己二烯 1,4-噁噻英,2,3-二氢-5,6-二甲基- 1,2-苯并噁噻英,3,4-二氢- 1,2-氧硫杂环己二烯 methyl 6-chlorosulfonyl-3-methyl-1,2-benzoxathiin 2,2-dioxide ethyl benzo[e][1,2]oxathiine-3-carboxylate 2,2-dioxide N,N,N',N'-tetramethyl-N''-[2,2,2-trichloro-1-(5',6'-dihydro-2'-methyl-1',4'-oxathiin-3'-carboxamido)ethyl]phosphoric triamide 4-tert-butyl-1-(2,2-dioxido-1,2-benzoxathiin-6-yl)-1H-1,2,3-triazole 2-amino-4a,5,6,7,8,8a-hexahydrobenzo[b][1,4]oxathiine-3-carbonitrile 2,3-dihydro-2-methyl-2,6-diphenyl-1,4-oxathiin 2-[1-(2,2-dioxido-1,2-benzoxathiin-6-yl)-1H-1,2,3-triazol-4-yl]propan-2-ol 5,6-dihydro-[1,2]oxathiine 2,2-dioxide (+/-)-(2R,3R)-3-[(5-acetyl-6-methyl-2-prop-2-enyloxy-2H,3H-1,4-oxathiin-3-yl)methylthio]pentane-2,4-dione 2-propyl-3-(chloroethyl)-5,6-dihydro-1,4-oxathiin 3-(2-chlorobutyl)-5,6-dihydro-2-methyl-1,4-oxathiin 3-(2-chloroethyl)-5,6-dihydro-2-methyl-1,4-oxathiin 1-<5,6-dihydro-2-methyl-6-N-(2'-oxo-2',3',4',5'-tetrahydropyrrolo)-1,4-oxathiin-3-yl>ethanone 3-(2-chloroethyl)-5,6-dihydro-1,4-oxathiin 2-Butanone, 4-(4-hydroxy-2,2-dioxido-1,2-benzoxathiin-3-yl)-4-phenyl- Phosphorodithioic acid, S-2,3-dihydro-1,4-oxathiinyl O,O-dimethyl ester 4,7-Dimethyl-1,2,5,6,7,8-hexahydro-1-oxa-2-thianaphthalene 2,2-dioxide 4,5,6,7,8,9-hexahydro-1H-cyclohept[d][1,2]oxathiin-3-oxide 6,8-dichloro-1,2-benzoxathiine 2,2-dioxide 6-Morpholin-4-yl-2-phenyl-4,5,6,7-tetrahydro-9-oxa-1,8-dithia-3-aza-cyclopenta[a]naphthalene 8,8-dioxide 2-Phenyl-6-piperidin-1-yl-4,5,6,7-tetrahydro-9-oxa-1,8-dithia-3-aza-cyclopenta[a]naphthalene 8,8-dioxide ocimene sultone N,N-diisopropyl-3,4,5,6-tetrahydro-8-phenyl-1,2-oxathiino<5,6-g>benzothiazol-4-amine 2,2-dioxide N,N-dimethyl-3,4,5,6-tetrahydro-8-phenyl-1,2-oxathiino<5,6-g>benzothiazol-4-amine 2,2-dioxide 1,4-dimethyl-5,6,7,8-tetrahydro-benz[d][1,2]oxathiin-3,3-dioxide 2,2-dioxido-1,2-benzoxathiin-6-yl methanesulfonate (5,6-Dihydro-[1,4]oxathiin-2-yl)-acetic acid methyl ester acetic acid 2,2-dioxo-2H-2λ6-benzo[e][1,2]oxathiin-7-yl ester methanesulfonic acid 2,2-dioxo-2H-2λ6-benzo[e][1,2]oxathiin-7-yl ester acetic acid 2,2-dioxo-3,4-dihydro-2H-2λ6-benzo[e][1,2]oxathiin-7-yl ester methanesulfonic acid 2,2-dioxo-3,4-dihydro-2H-2λ6-benzo[e][1,2]oxathiin-7-yl ester ethyl 5,6-dihydro-2-trifluoromethyl-1,4-oxathiin-3-carboxylate 6-Phenyl-1,4-oxathiin-2-one 4-cyclopropyl-1-(2,2-dioxido-1,2-benzoxathiin-6-yl)-1H-1,2,3-triazole 4-(N,N-Diethylamino)-3,4,10,11-tetrahydro-5H-benzo-cyclohepta-1,2-oxathiin-2,2-dioxid (2,2-Dioxo-2,3,4,5,6,7-hexahydro-1-oxa-2λ6-thia-dibenzo[a,c]cyclohepten-4-yl)-diethyl-amine 6-methyl-4-pyrrolidin-1-yl-3,4,5,6,7,8-hexahydro-[1,2]oxathiino[5,6-c]pyridine 2,2-dioxide 6-methyl-4-piperidin-1-yl-3,4,5,6,7,8-hexahydro-[1,2]oxathiino[5,6-c]pyridine 2,2-dioxide 1-(2,2-Dioxo-6-phenyl-3,4-dihydro-2H-2λ6-[1,2]oxathiin-4-yl)-piperidine