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O,O'-sulfinyl-tartaric acid diethyl ester | 133522-25-5

中文名称
——
中文别名
——
英文名称
O,O'-sulfinyl-tartaric acid diethyl ester
英文别名
Thionyl-mesoweinsaeure-diaethylester;O,O'-Sulfinyl-weinsaeure-diaethylester;Diethyl 2-oxo-1,3,2-dioxathiolane-4,5-dicarboxylate
<i>O</i>,<i>O'</i>-sulfinyl-tartaric acid diethyl ester化学式
CAS
133522-25-5
化学式
C8H12O7S
mdl
——
分子量
252.245
InChiKey
RHWWCXCJNYQHMA-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):
    0.6
  • 重原子数:
    16
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    107
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

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文献信息

  • NONAQUEOUS ELECTROLYTE, CAPACITOR DEVICE USING SAME, AND CARBOXYLIC ACID ESTER COMPOUND USED IN SAME
    申请人:UBE Industries, Ltd.
    公开号:EP3086396A1
    公开(公告)日:2016-10-26
    The present invention provides a nonaqueous electrolytic solution capable of improving electrochemical characteristics in the case of using an energy storage device at a high temperature and at a high voltage and further capable of inhibiting the gas generation while maintaining a capacity retention rate after storage at a high temperature and at a high voltage and also provides an energy storage device using the same. Disclosed is a nonaqueous electrolytic solution having an electrolyte salt dissolved in a nonaqueous solvent, the nonaqueous electrolytic solution containing a carboxylic acid ester compound represented by the following general formula (I). In the formula, each of R1 and R2 independently represents a hydrogen atom, a -C(=O)-OR4 group, or the like, and R1 and R2 may be bonded to each other to form a ring structure. R3 represents a hydrogen atom or the like, and n represents an integer of 1 to 3. When n is 1, then L and R4 represent an alkyl group having 1 to 6 carbon atoms or the like; and when n is 2 or 3, then L represents an n-valent connecting group, X represents a -C(=O)- group, an -S(=O)-group, an -S(=O)2- group, an -S(=O)2-R5-S(=O)2- group or a CR6R7 group, R5 represents an alkylene group having 1 to 4 carbon atoms, and each of R6 and R7 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
    本发明提供了一种非水性电解溶液,该溶液能够改善在高温高压下使用储能装置时的电化学特性,并且能够进一步抑制气体生成,同时在高温高压下储存后保持容量保持率,本发明还提供了使用该溶液的储能装置。本发明公开了一种非水电解溶液,该溶液具有溶解在非水溶剂中的电解质盐,该非水电解溶液含有由以下通式(I)代表的羧酸酯化合物。 式中,R1 和 R2 各自独立地代表氢原子、-C(=O)-OR4 基团或类似基团,R1 和 R2 可相互键合以形成环状结构。R3 代表氢原子或类似物,n 代表 1 至 3 的整数。当 n 为 1 时,L 和 R4 代表具有 1 至 6 个碳原子的烷基或类似基团;当 n 为 2 或 3 时,L 代表 n 价连接基团,X 代表 -C(=O)- 基团、-S(=O)- 基团、-S(=O)2- 基团、-S(=O)2-R5-S(=O)2- 基团或 CR6R7 基团,R5 代表具有 1 至 4 个碳原子的亚烷基,R6 和 R7 分别代表氢原子或具有 1 至 6 个碳原子的烷基。
  • Nonaqueous electrolyte, capacitor device using same, and carboxylic acid ester compound used in same
    申请人:UBE INDUSTRIES, LTD.
    公开号:US10263285B2
    公开(公告)日:2019-04-16
    The present invention provides a nonaqueous electrolytic solution capable of improving electrochemical characteristics in the case of using an energy storage device at a high temperature and at a high voltage and further capable of inhibiting the gas generation while maintaining a capacity retention rate after storage at a high temperature and at a high voltage and also provides an energy storage device using the same. Disclosed is a nonaqueous electrolytic solution having an electrolyte salt dissolved in a nonaqueous solvent, the nonaqueous electrolytic solution containing a carboxylic acid ester compound represented by the following general formula (I). In the formula, each of R1 and R2 independently represents a hydrogen atom, a —C(═O)—OR4 group, or the like, and R1 and R2 may be bonded to each other to form a ring structure. R3 represents a hydrogen atom or the like, and n represents an integer of 1 to 3. When n is 1, then L and R4 represent an alkyl group having 1 to 6 carbon atoms or the like; and when n is 2 or 3, then L represents an n-valent connecting group, X represents a —C(═O)— group, an —S(═O)— group, an —S(═O)2— group, an —S(═O)2—R5—S(═O)2— group or a CR6R7 group, R5 represents an alkylene group having 1 to 4 carbon atoms, and each of R6 and R7 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
    本发明提供了一种非水性电解溶液,该溶液能够改善在高温高压下使用储能装置时的电化学特性,并且能够进一步抑制气体生成,同时在高温高压下储存后保持容量保持率,本发明还提供了使用该溶液的储能装置。本发明公开了一种非水电解溶液,该溶液具有溶解在非水溶剂中的电解质盐,该非水电解溶液含有由以下通式(I)代表的羧酸酯化合物。 式中,R1 和 R2 各自独立地代表氢原子、-C(═O)-OR4 基团或类似基团,R1 和 R2 可相互键合以形成环状结构。R3 代表氢原子或类似物,n 代表 1 至 3 的整数。当 n 为 1 时,L 和 R4 代表具有 1 至 6 个碳原子的烷基或类似基团;当 n 为 2 或 3 时,L 代表 n 价连接基团,X 代表-C(═O)-基团、-S(═O)-基团、-S(═O)2-基团、-S(═O)2-R5-S(═O)2-基团或 CR6R7 基团,R5 代表具有 1 至 4 个碳原子的亚烷基,R6 和 R7 分别代表氢原子或具有 1 至 6 个碳原子的烷基。
  • Wood; Nicholas, Journal of the Chemical Society, 1928, p. 1714
    作者:Wood、Nicholas
    DOI:——
    日期:——
  • Rao; Guha, Chemische Berichte, 1934, vol. 67, p. 743,746
    作者:Rao、Guha
    DOI:——
    日期:——
  • McKenzie; Barrow, Journal of the Chemical Society, 1911, vol. 99, p. 1923,1924
    作者:McKenzie、Barrow
    DOI:——
    日期:——
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同类化合物

环丙基亚磺酸酯 亚硫酸丙烯酯 亚硫酸丁烯酯 亚硫酸丁烯酯 亚硫酸丁烯酯 5-异丙基-1,3,2-二氧硫杂环己烷2-氧化物 4-甲基-1,3,2-二恶噻戊环-4-甲酰氯2-氧化物 4,4-二甲基-1,3,2-二氧硫杂环己烷2-氧化物 2,4,8,10-四氧杂-3,9-二硫杂螺[5.5]十一烷3,9-二氧化物 (4S)-4-甲基-2-氧代-[1,3,2]二恶噻戊环-4-羧酸甲酯 (4S,5R)-4-ethoxycarbonyl-5-pentadecyl-1,3,2-dioxathiolane-2-oxide 1,3,2-Dioxathiane, 5-ethyl-5-propyl-, 2-oxide 5-Ethyl-5-phenyl-[1,3,2]dioxathiane 2-oxide 5,5-diethyltrimethylene sulphite 5-Butyl-5-ethyl-[1,3,2]dioxathiane 2-oxide Glykolsaeure-anhydrosulfit 2-Methyl-2-nitro-propan-1,3-diol-sulfit 5-Methyl-trimethylensulfit ethyl 2-oxo-5-thiophen-2-yl-2λ4-[1,3,2]dioxathiolane-4-carboxylic acid ethyl ester 2-Methyl-2-propyl-propan-1,3-diyl-sulfit 4,6-Diisopropyl-2-oxo-1,3,2-dioxathian 5,5-Dimethyl-1,3,2-dioxathian 2-ethyl-2-chloromethyltrimethylene sulfite diallyl (4R,5R)-1,3,2-dioxathiolane-4,5-dicarboxylate 2-oxide 5-nitro-5-chloromethyl-2-thia-1,3-dioxane 2-oxide 5-nitro-5-hydroxymethyl-2-thia-1,3-dioxane 2-oxide 4,6-Dimethyltrimethylensulfit β-Chlor-α-hydroxy-α-methyl-propionsaeure-anhydrosulfit methyl (4R)-4-methyl-2-oxo-2λ4-[1,3,2]dioxathiolane-4-carboxylate 4,4,6-trimethyltrimethylene sulphite 4,6-dimethyltrimethylene (cis,trans) sulphite 4-methyl-[1,3,2]dioxathiane cis-2-oxide 5-Ethyl-5-(sulfinylamino)-1,3,2-dioxathiane 2-oxide 4,4,5,6,6-pentamethyl-1,3,2-dioxathian 2-oxide dimethyl (4R,5R)-1,3,2-dioxathiolane-4,5-dicarboxylate 2-oxide 2,4-O-benzylidene-D-erythritol 1,3-cyclic sulfite 4,4-dimethyltrimethylenesulphite 4,4,6,6-tetramethyltrimethylene sulphite ethyl (4R,5S)-5-[[(4S,5S)-5-azido-2-phenyl-1,3-dioxan-4-yl]methyl]-2-oxo-1,3,2-dioxathiolane-4-carboxylate 4,6-dimethyltrimethylene (cis,cis) sulphite α-Hydroxy-α-ethyl-buttersaeure-anhydrosulfit 4-Phenyl-trimethylensulfit trans-5-tert-butyl-r-2-oxo-1,3,2-dioxathiane (S)-4-methyl-2-oxo-2λ4-[1,3,2]dioxathiolane-4-carboxylic acid N-methoxy-N-methylamide Cyclischer Sulfitester des 2-Methyl-2-sulfinylamino-propan-1,3-diols (4R,5S)-methyl 5-phenyl-2-thioxo-1,3-dioxolane-4-carboxylate Methyl 4-methyl-2-oxo-1,3,2lambda~4~-dioxathiolane-4-carboxylate 1,3,5-Dioxathiane 2,5-Dioxo-1,3,2lambda~4~-dioxathiolane-4-carboxylic acid 1,3,2-Dioxathian