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2.2-Dinitro-trimethylen-sulfit (5.5-Dinitro-1.3-dioxa-2-thia-cyclohexan-2-oxid) | 25797-50-6

中文名称
——
中文别名
——
英文名称
2.2-Dinitro-trimethylen-sulfit (5.5-Dinitro-1.3-dioxa-2-thia-cyclohexan-2-oxid)
英文别名
5,5-dinitro-[1,3,2]dioxathiane 2-oxide;5,5-Dinitro-1,3,2-dioxathiane 2-oxide
2.2-Dinitro-trimethylen-sulfit (5.5-Dinitro-1.3-dioxa-2-thia-cyclohexan-2-oxid)化学式
CAS
25797-50-6
化学式
C3H4N2O7S
mdl
——
分子量
212.14
InChiKey
CRABLNABLJSMEI-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):
    -0.3
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    146
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    参考文献:
    名称:
    gem-Dinitro Esters. IV. Pyridine-Catalyzed Esterification of β-Dinitro Alcohols1
    摘要:
    DOI:
    10.1021/jo01044a537
  • 作为产物:
    描述:
    2,2-二硝基丙烷-1,3-二醇吡啶 氯化亚砜 作用下, 以 二氯甲烷 为溶剂, 反应 2.83h, 以82%的产率得到2.2-Dinitro-trimethylen-sulfit (5.5-Dinitro-1.3-dioxa-2-thia-cyclohexan-2-oxid)
    参考文献:
    名称:
    Synthesis of an Azido Energetic Alcohol
    摘要:
    一种制备偶氮基能量醇的方法包括将偶氮基二醇转化为环状亚磺酸酯,将环状亚磺酸酯氧化为环状硫酸酯,然后打开环状硫酸酯。接着,打开环状硫酸酯并进行水解,以形成偶氮基能量醇。
    公开号:
    US20110319643A1
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文献信息

  • Synthesis of an Azido Energetic Alcohol
    申请人:Thompson Alicia
    公开号:US20110319643A1
    公开(公告)日:2011-12-29
    A method of forming an azido energetic alcohol includes converting an energetic diol to a cyclic sulfite, oxidizing the cyclic sulfite to a cyclic sulfate, and opening the cyclic sulfate. The cyclic sulfate is opened, followed by hydrolysis, to form an azido energetic alcohol.
    一种制备偶氮基能量醇的方法包括将偶氮基二醇转化为环状亚磺酸酯,将环状亚磺酸酯氧化为环状硫酸酯,然后打开环状硫酸酯。接着,打开环状硫酸酯并进行水解,以形成偶氮基能量醇。
  • gem-Dinitro Esters. IV. Pyridine-Catalyzed Esterification of β-Dinitro Alcohols<sup>1</sup>
    作者:L. W. Kissinger、T. M. Benziger、H. E. Ungnade、R. K. Rohwer
    DOI:10.1021/jo01044a537
    日期:1963.9
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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