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6-Benzyl-2,3-dihydro-1,4-oxathiine-5-carboxamide

中文名称
——
中文别名
——
英文名称
6-Benzyl-2,3-dihydro-1,4-oxathiine-5-carboxamide
英文别名
6-benzyl-2,3-dihydro-1,4-oxathiine-5-carboxamide
6-Benzyl-2,3-dihydro-1,4-oxathiine-5-carboxamide化学式
CAS
——
化学式
C12H13NO2S
mdl
——
分子量
235.3
InChiKey
WINKBFJSWXNELC-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):
    1.3
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    77.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] PESTICIDALLY ACTIVE BICYCLIC HETEROCYCLES WITH SULPHUR CONTAINING SUBSTITUENTS<br/>[FR] HÉTÉROCYCLES BICYCLIQUES PESTICIDEMENT ACTIFS COMPORTANT DES SUBSTITUANTS CONTENANT DU SOUFRE
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2015071180A1
    公开(公告)日:2015-05-21
    Compounds of the formula (I), and the agrochemically acceptable salts and N-oxides of those compounds, including all stereoisomers and tautomeric forms, and wherein the substituents are as defined in claim 1, are useful for controlling animal pests and can be prepared in a manner known per se.
    化合物的公式(I),以及这些化合物的农药可接受的盐和N-氧化物,包括所有立体异构体和互变异构体形式,其中取代基如权利要求1中定义的,对于控制动物害虫是有用的,并且可以按照已知的方法制备。
  • [EN] PESTICIDALLY ACTIVE SUBSTITUTED 5,5-BICYCLIC HETEROCYCLES WITH SULPHUR CONTAINING SUBSTITUENTS<br/>[FR] HÉTÉROCYCLES 5,5-BICYCLIQUES SUBSTITUÉS À ACTION PESTICIDE POSSÉDANT DES SUBSTITUANTS SOUFRÉS
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2015091945A1
    公开(公告)日:2015-06-25
    Compounds of the formula (I) and the agrochemically acceptable salts, stereoisomers, enantiomers, tautomers and N-oxides of those compounds, including all stereoisomers and tautomeric forms, and wherein the substituents are as defined in claim 1, are useful for controlling animal pests and can be prepared in a manner known per se.
    公式(I)的化合物及农药可接受的盐、立体异构体、对映异构体、互变异构体和这些化合物的N-氧化物,包括所有立体异构体和互变异构体形式,在其中取代基如权利要求1中定义的,用于控制动物害虫,并可以按照已知的方法制备。
  • [EN] FUNGICIDAL PYRIMIDINE COMPOUNDS<br/>[FR] COMPOSÉS FONGICIDES DE PYRIMIDINE
    申请人:BASF SE
    公开号:WO2015036059A1
    公开(公告)日:2015-03-19
    The present invention relates to fungicidal pyrimidine compounds (I), to their use and to methods for combating phytopathogenic fungi. The present invention also relates to mixtures and compositions comprising compounds I and to seed treated with at least one compound (I). Furthermore the invention relates to processes for preparing compounds of formula (I).
    本发明涉及杀菌嘧啶化合物(I),其使用以及用于对抗植物病原真菌的方法。本发明还涉及包含化合物I的混合物和组合物,以及至少用一种化合物(I)处理的种子。此外,本发明还涉及制备式(I)化合物的方法。
  • COMPOSITIONS COMPRISING A TRIAZOLE COMPOUND
    申请人:BASF SE
    公开号:EP2934146A1
    公开(公告)日:2015-10-28
  • SYNERGISTIC FUNGICIDAL COMPOSITIONS CONTAINING KHC03
    申请人:BASF SE
    公开号:EP3051948A1
    公开(公告)日:2016-08-10
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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