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2,3-dihydro-6-methyl-1,4-oxathiin | 102363-66-6

中文名称
——
中文别名
——
英文名称
2,3-dihydro-6-methyl-1,4-oxathiin
英文别名
6-Methyl-2,3-dihydro-1,4-benzoxathiine
2,3-dihydro-6-methyl-1,4-oxathiin化学式
CAS
102363-66-6
化学式
C9H10OS
mdl
——
分子量
166.244
InChiKey
UHPJCGVOCBGWON-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

  • 沸点:
    113-115 °C(Press: 3.5 Torr)
  • 密度:
    1.162±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:5668f6b70404187c4cf42018edcc2e66
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反应信息

  • 作为反应物:
    描述:
    2,3-dihydro-6-methyl-1,4-oxathiin磺酰氯双氧水溶剂黄146 作用下, 以 二氯甲烷 为溶剂, 生成 6-Methyl-benzo[1,4]oxathiine 4,4-dioxide
    参考文献:
    名称:
    磷酸酪氨酸模拟物的设计与合成。
    摘要:
    蛋白质酪氨酸磷酸酶(PTPases)的选择性抑制剂作为治疗剂和研究工具备受关注。成功合成了几种设计为磷酸酪氨酸模拟物或不可逆活性位点抑制剂的苯丙氨酸衍生物(1、2),然后将其结合到基于拟肽β链模板的组合文库中。
    DOI:
    10.1016/s0960-894x(03)00253-1
  • 作为产物:
    描述:
    6-Methyl-2,3,5,6,7,8-hexahydro-benzo[1,4]oxathiine 在 N-溴代丁二酰亚胺(NBS) 作用下, 以 四氯化碳 为溶剂, 反应 1.0h, 以72%的产率得到2,3-dihydro-6-methyl-1,4-oxathiin
    参考文献:
    名称:
    Mursakulov, I. G.; Ramazanov, E. A.; Kerimov, F. F., Journal of Organic Chemistry USSR (English Translation), 1990, vol. 26, # 1.2, p. 113 - 116
    摘要:
    DOI:
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文献信息

  • [EN] HETEROBICYCLE-SUBSTITUTED AZOLYL BENZENE FUNGICIDES<br/>[FR] FONGICIDES D'AZOLYL BENZÈNE SUBSTITUÉ PAR HÉTÉROBICYCLE
    申请人:DU PONT
    公开号:WO2011059619A1
    公开(公告)日:2011-05-19
    Disclosed are compounds of Formula 1, including all stereoisomers, N oxides, and salts thereof, wherein Y is a 5-membered, fully or partially unsaturated heterocyclic ring containing 2-4 carbon atoms and 2-3 nitrogen atoms as ring members, the ring substituted with Z on a ring member atom connected through an adjacent single ring member atom to the ring member atom attaching the heterocyclic ring to the phenyl ring of Formula 1, and optionally further substituted with up to 2 substituents independently selected from R5 on carbon atom ring members and from R6 on nitrogen atom ring members; Z is an 8-, 9-, 10- or 11-membered fused heterobicyclic ring system containing ring members selected from carbon atoms and 1 to 4 heteroatoms independently selected from up to 2 O, up to 2 S and up to 4 N atoms, wherein up to 3 carbon atom ring members are independently selected from C(=O) and C(=S), and the sulfur atom ring members are independently selected from S(=O)u(=NR7)z, the ring system optionally substituted with substituents independently selected from R8 on carbon atom ring members and from R9 on nitrogen atom ring members; and R1, R2, R3, R4, R5, R6, R7, R8, R9, u and z are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 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.
    公开的是Formula 1的化合物,包括所有立体异构体、N-氧化物和盐,其中Y是一个5元的、完全或部分不饱和的杂环环,含有2-4个碳原子和2-3个氮原子作为环成员,该环在通过相邻的单环成员原子连接到将杂环环连接到Formula 1的苯环上的环成员原子上与Z取代,并且可选地进一步取代最多2个取代基,独立地从碳原子环成员上的R5和氮原子环成员上的R6中选择;Z是一个8、9、10或11元的融合杂双环环系统,其中环成员从碳原子和1到4个异原子中独立选择,这些异原子最多选择2个O、最多2个S和最多4个N原子,其中最多3个碳原子环成员独立选择自C(=O)和C(=S),硫原子环成员独立选择自S(=O)u(=NR7)z,环系统可选地取代取代基,独立地从碳原子环成员上的R8和氮原子环成员上的R9中选择;以及R1、R2、R3、R4、R5、R6、R7、R8、R9、u和z如披露中所定义。还公开了含有Formula 1的化合物的组合物以及用于控制由真菌病原体引起的植物病害的方法,包括施用本发明的化合物或组合物的有效量。
  • C-ARYL GLUCOSIDE DERIVATIVE, PREPARATION METHODS THEREOF, AND MEDICAL APPLICATIONS THEREOF
    申请人:JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD.
    公开号:US20160222047A1
    公开(公告)日:2016-08-04
    C-aryl glucoside derivatives, preparation methods thereof, and medical applications thereof are described. Specifically, compounds represented by formula I, and, tautomers, enantiomers, diastereomers, racemates, and pharmaceutically acceptable salts of the compounds, preparation methods thereof, pharmaceutical compositions containing the compounds, and applications thereof are described. Compounds of formula (I) are useful as therapeutic agents, and particularly as sodium-dependent glucose contransporter protein (SGLT) inhibitors.
    本文描述了C-芳基葡萄糖苷衍生物,其制备方法以及医药应用。具体而言,描述了由式I表示的化合物,以及该化合物的互变异构体、对映体、非对映体、拉卡酯和药学上可接受的盐,其制备方法,含有该化合物的药物组合物以及其应用。式(I)的化合物可用作治疗剂,特别是作为钠依赖葡萄糖共转运蛋白(SGLT)抑制剂。
  • [EN] 6-ACYL-1,2,4-TRIAZINE-3,5-DIONE DERIVATIVE AND HERBICIDES<br/>[FR] DÉRIVÉ 6-ACYL-1,2,4-TRIAZINE-3,5-DIONE ET HERBICIDES
    申请人:KUMIAI CHEMICAL INDUSTRY CO
    公开号:WO2012002096A1
    公开(公告)日:2012-01-05
    Disclosed are compounds exhibiting sufficient herbicidal activity at low application dosage when they are applied to soils and foliage, and an agrochemical composition using the same, in particular herbicides. The compounds are triazine derivatives represented by following Formula 1 or salts thereof, and the herbicides containing them: [Chem. 28] wherein in the formula, R1 represents a hydrogen atom; a C1-C12 alkyl group; a C2-C6 alkenyl group, etc., R2 represents a C1-C12 alkyl group, etc., Y and Z represent an oxygen atom or a sulfur atom, and A represents a 5- or 6-membered cyclic group which may contain a nitrogen atom, an oxygen atom, or a sulfur atom.
    本公开了一种在施加于土壤和叶面时表现出足够的除草活性的化合物,以及使用这些化合物的农药组合物,特别是除草剂。这些化合物是由以下化学式1所代表的三嗪衍生物或其盐,以及含有它们的除草剂:[Chem. 28] 在该式中,R1代表氢原子;C1-C12烷基;C2-C6烯基等,R2代表C1-C12烷基等,Y和Z代表氧原子或硫原子,A代表可能含有氮原子、氧原子或硫原子的5-或6-成员环状基团。
  • A new route to 2,3-dihydro-1,4-benzoxathiine and 2,3-dihydro-1,4-benzodithiine
    作者:James Y. Satoh、Amos M. Haruta、Christopher T. Yokoyama、Yasuo Yamada、Masakatsu Hirose
    DOI:10.1039/c39850001645
    日期:——
    The ethylene monothioacetals and dithioacetals of alkylcyclohexanones react with copper(II) bromide to give 2,3-dihydro-1,4-benzoxathiine and 2,3-dihydro-1,4-benzodithiine derivatives, respectively.
    烷基环己酮的乙烯单硫缩醛和二硫缩醛与溴化铜(II)反应,分别得到2,3-二氢-1,4-苯并benzo啶和2,3-二氢-1,4-苯并二硫胺衍生物。
  • [EN] FUNGICIDAL TETRAZOLINONES<br/>[FR] TÉTRAZOLINONES FONGICIDES
    申请人:DU PONT
    公开号:WO2015191382A1
    公开(公告)日:2015-12-17
    Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein R1, R2, R3, R4a, R4b, W and Z are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 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.
    本发明涉及一种公式1的化合物,包括所有立体异构体、N-氧化物和其盐,其中R1、R2、R3、R4a、R4b、W和Z如所述。本发明还涉及含有公式1化合物的组合物以及控制由真菌病原体引起的植物病害的方法,包括施用本发明中化合物或组合物的有效量。
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