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2-Isopropyl-1,3-oxathian | 24699-59-0

中文名称
——
中文别名
——
英文名称
2-Isopropyl-1,3-oxathian
英文别名
1,3-Oxathiane, 2-(1-methylethyl)-;2-propan-2-yl-1,3-oxathiane
2-Isopropyl-1,3-oxathian化学式
CAS
24699-59-0
化学式
C7H14OS
mdl
——
分子量
146.254
InChiKey
FKKNDMYFFMTCTQ-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):
    2.4
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-Isopropyl-1,3-oxathian二叔丁基过氧化物 作用下, 以 氯苯 为溶剂, 反应 4.0h, 以65%的产率得到1-Propyl thioisobutyrate
    参考文献:
    名称:
    Zorin, V. V.; Batyrbaev, N. A.; Zlot-skii, S. S., Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, p. 347 - 352
    摘要:
    DOI:
  • 作为产物:
    描述:
    Lithium, 1,3-oxathian-2-yl- 以35%的产率得到
    参考文献:
    名称:
    FUJI K.; UEDA M.; FUJITA E., J. CHEM. SOC. CHEM. COMMUNS , 1977, NO 22,
    摘要:
    DOI:
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文献信息

  • Substituted Amidine Compounds for Combating Animal Pests
    申请人:Kaiser Florian
    公开号:US20110257011A1
    公开(公告)日:2011-10-20
    The invention relates to substituted amidine compounds of formula (I), to the enantiomers, diastereomers and salts thereof and to compositions comprising such compounds. The invention also relates to the use of the substituted amidine compounds, of their salts or of compositions comprising them for combating animal pests. Furthermore the invention relates also to methods of applying such substituted amidine compounds. The substituted amidine compounds of the present invention are defined by the following formula I: wherein A 1 to A 4 , B 1 to B 3 , R 1 to R 3 , (R 4 ) p , (R 5 ) q , X and Y are defined as in the description.
    本发明涉及公式(I)的取代氨基化合物,其对映异构体、对映异构体和其盐以及含有这种化合物的组合物。本发明还涉及使用取代氨基化合物、其盐或含有它们的组合物来对抗动物害虫。此外,本发明还涉及应用这种取代氨基化合物的方法。本发明的取代氨基化合物由以下公式I定义:其中A1到A4,B1到B3,R1到R3,(R4)p,(R5)q,X和Y如描述中所定义。
  • Substituted ketonic isoxazoline compounds and derivatives for combating animal pests
    申请人:Koerber Karsten
    公开号:US20120309620A1
    公开(公告)日:2012-12-06
    The invention relates to substituted ketonic isoxazoline compounds of formula (I), to the enantiomers, diastereomers and salts thereof and to compositions comprising such compounds. The invention also relates to the use of the substituted ketonic isoxazoline compounds, of their salts or of compositions comprising them for combating animal pests. Furthermore the invention relates also to methods of applying such substituted ketonic isoxazoline compounds. The substituted ketonic isoxazoline compounds of the present invention are defined by the following formula I: wherein A 1 to A 4 , R 1 to R 3 , (R 4 ) p , (R 5 ) q , X and (G) m are defined as in the description.
    本发明涉及式(I)的取代酮异噁唑化合物,其对映异构体、二对映异构体和盐,以及包含这些化合物的组合物。本发明还涉及使用所述取代酮异噁唑化合物、其盐或包含它们的组合物来对抗动物害虫。此外,本发明还涉及应用这些取代酮异噁唑化合物的方法。本发明的取代酮异噁唑化合物由以下式(I)定义:其中A1至A4、R1至R3、(R4)p、(R5)q、X和(G)m的定义如描述中所示。
  • Reductions with metal-ammonia combinations. II. Monothioacetals and monothioketals. Synthesis of alkoxymercaptans
    作者:Ernest L. Eliel、Terrence W. Doyle
    DOI:10.1021/jo00833a052
    日期:1970.8
  • Chemistry of carbanions stabilized by sulfur. 1. Chemistry of 1,3-oxathianes. Synthesis and conformation of 2-substituted 1,3-oxathianes
    作者:Kaoru Fuji、Masaru Ueda、Kenzo Sumi、Kanji Kajiwara、Eiichi Fujita、Takashi Iwashita、Iwao Miura
    DOI:10.1021/jo00205a020
    日期:1985.3
  • ZORIN, V. V.;BATYRBAEV, N. A.;ZLOTSKIJ, S. S.;RAXMANKULOV, D. L., ZH. ORGAN. XIMII, 1984, 20, N 2, 387-393
    作者:ZORIN, V. V.、BATYRBAEV, N. A.、ZLOTSKIJ, S. S.、RAXMANKULOV, D. L.
    DOI:——
    日期:——
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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cnmr
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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同类化合物

硫代羟基乙酸酐 二乙氧基-(1,4-恶噻烷-3-基硫基)-硫代膦烷 6-异丙基-1,4-恶噻烷-2-酮 5-异丙基-2-甲基-1,3-氧硫杂环已烷 4,4-二氢-4-亚氨基-1,4-氧硫杂环己烷 4-氧化物 3,4-环氧四氢噻吩-1,1-二氧化物 2-甲基-4-正丙基-1,3-氧硫杂环己烷 2-甲基-1,4-氧硫杂环已烷4,4-二氧化物 2-甲基-1,3-氧硫杂环已烷 2-异丙基-5-甲基-1,3-氧硫杂环已烷 2,6-二甲基-1,4-氧硫杂环己烷 2,6-二甲基-1,3-氧硫杂环已烷 1-甲基-6-氧杂-3-硫杂双环[3.1.0]己烷3,3-二氧化物 1-氧杂-4-硫杂螺[4.5]癸烷-2-甲醇氨基甲酸酯 1,4-氧硫杂环已烷4-氧化物 1,4-恶噻烷-2-酮 1,4-噻烷-1,1-二氧 1,4-噻烷 1,4-丁磺酸内酯 1,3-氧硫杂环已烷 1,2-氧杂硫烷,3,3,4,4,5,5,6,6-八氟-,2,2-二氧化 ethyl 2-c-phenyl-3-triethylsilyl-1,4-oxathiane-3-r-carboxylate ethyl cis-2-phenyl-3-(triethylsilyl)-1,4-oxathiane-3-carboxylate (4SR,4aSR,8aSR)-8a-methylhexahydrobenzo[b][1,4]oxathiin-2-one S-oxide 4,4-dimethyl-2-(1-methyl-butyl)-1,3-oxathiane 7,7-dichloro-1,6-dimethyl-2-oxa-5-thiabicyclo<4.1.0>heptane methyl trans-2-phenyl-1,4-oxathiane-3-carboxylate 4-oxathiane-2,6-dione endo-4-oxa-3-thia-tricyclo[6.2.2.02,7]dodec-9-ene 3,3-dioxide (1,4-oxathian-2-yl)acetaldehyde 2,2,3,3-tetramethyl-1,4-oxathiane N-(6-methyl-1,4-oxathian-3-ylidene)benzenamine N-(6-phenyl-1,4-oxathian-3-ylidene)benzenamine 2,7-dioxa-3-oxo-5-thia-bicyclo[2.2.1] heptane trimethylene monothiocarbonate 4-Methylene-1-oxa-2-thia-spiro[5.5]undecane 2-oxide 3-(3-thienyl)-1,4-oxathiane trans-octahydro-2H-cyclohepta[b][1,4]oxathiin-2-one 1,7-dioxa-5,11-dithiaspiro[5.5]undecane 4,4-dimethyl-2-(2-phenyl-propyl)-1,3-oxathiane 2-decyl-4,4-dimethyl-1,3-oxathiane methl 2,5-anhydro-2-thio-β-D-lyxofuranoside 2-phenyl-3-trifluoromethyl-1,4-oxathiinane-3-carboxylic acid methyl ester (1R,3R,4S,7R,8R,11R)-4-methyl-3,8,11-triphenyl-2,9-dioxa-10-thia-5-azatricyclo[5.2.2.01,5]undecan-6-one 4-Hydroxy-1-methylbutansulfonsaeure 1,4-Sulton 4-(1-Carboxy-ethyl)-1,4-oxathianiumbromid 2-(Pent-2-en-1-yl)-4-propyl-1,3-oxathiane 3,3,5-Trichloro-1,4-oxathiane 2,3,3,5-Tetrachloro-1,4-oxathiane 2,3,3-Trichloro-1,4-oxathiane