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(2,2-Dihydroxyoxathian-3-yl) ethyl carbonate

中文名称
——
中文别名
——
英文名称
(2,2-Dihydroxyoxathian-3-yl) ethyl carbonate
英文别名
(2,2-dihydroxyoxathian-3-yl) ethyl carbonate
(2,2-Dihydroxyoxathian-3-yl) ethyl carbonate化学式
CAS
——
化学式
C7H14O6S
mdl
——
分子量
226.25
InChiKey
AKQZIYQGQXZMRI-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:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    86.2
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • NON-AQUEOUS ELECTROLYTIC SOLUTION, ELECTRICAL STORAGE DEVICE UTILIZING SAME, AND CYCLIC SULFONIC ACID ESTER COMPOUND
    申请人:Ube Industries, Ltd.
    公开号:EP2704246A1
    公开(公告)日:2014-03-05
    An object of the present invention is to provide a nonaqueous electrolytic solution capable of improving electrochemical characteristics in a broad temperature range, an energy storage device using it. A nonaqueous electrolytic solution of an electrolyte salt dissolved in a nonaqueous solvent, which comprises at least one cyclic sulfonic acid ester compound represented by the following general formula (I), and an energy storage device. (wherein R1 and R2 may be the same or different, each representing a hydrogen atom, an alkyl group in which at least one hydrogen atom may be substituted with a halogen atom, or a halogen atom; L represents a divalent hydrocarbon group of an alkylene group in which at least one hydrogen atom is substituted with OR3, or a divalent hydrocarbon group of an alkylene group in which at least one methylene (CH2) is substituted with C(=O); R3 represents a formyl group, an alkylcarbonyl group, an alkenylcarbonyl group, an alkenylcarbonyl group, an arylcarbonyl group, an alkoxycarbonyl group, an alkenyloxycarbonyl group, an alkynyloxycarbonyl group, an aryloxycarbonyl group, a 2,2-dioxide-1,2-oxathiolan-4-yloxycarbonyl group, a 2,2-dioxide-1,2-oxathian-4-yloxycarbonyl group, an alkanesulfonyl group, an arylsulfonyl group, a dialkylphosphoryl group, an alkoxy(alkyl)phosphoryl group, a dialkoxyphosphoryl group, -S(O)-OR4, or -C(O)CH2P(O)(OR5)2; R4 represents an alkyl group, a 2,2-dioxide-1,2-oxathiolan-4-yl group, or a 2,2-dioxide-1,2-oxathian-4-yl group; R5 represents an alkyl group; further, in R3, at least one hydrogen atom may be substituted with a halogen atom, and L may be further substituted with any of an alkyl group, a haloalkyl group or a halogen atom).
    本发明的目的是提供一种能够在宽温度范围内改善电化学特性的非水性电解溶液,以及使用该溶液的储能装置。 一种溶解在非水溶剂中的电解质盐的非水性电解溶液,它包含至少一种由以下通式(I)表示的环磺酸酯化合物,以及一种储能装置。 (其中 R1 和 R2 可以相同或不同,各自代表氢原子、其中至少一个氢原子可被卤素原子取代的烷基或卤素原子;L 代表其中至少一个氢原子被 OR3 取代的亚烷基的二价烃基,或其中至少一个亚甲基 (CH2) 被 C(=O) 取代的亚烷基的二价烃基;R3 代表甲酰基、烷基羰基、烯基羰基、芳基羰基、烷氧基羰基、烯氧基羰基、炔氧基羰基、芳氧基羰基、2,2-二氧-1、2-氧硫杂环戊-4-基氧基羰基、2,2-二氧-1,2-氧硫杂环戊-4-基氧基羰基、烷基磺酰基、芳基磺酰基、二烷基磷酰基、烷氧基(烷基)磷酰基、二烷氧基磷酰基、-S(O)-OR4 或 -C(O)CH2P(O)(OR5)2;R4 代表烷基、2,2-二氧代-1,2-氧硫杂环戊-4-基或 2,2-二氧代-1,2-氧硫杂环戊-4-基;R5 代表烷基;此外,在 R3 中,至少一个氢原子可被卤素原子取代,L 可进一步被烷基、卤代烷基或卤素原子中的任何一个取代。)
  • US9608287B2
    申请人:——
    公开号:US9608287B2
    公开(公告)日:2017-03-28
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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