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ethyl (4S,5R)-4-carbethoxy-5-phenyl-1,3,2-dioxathiolane-2-oxide | 172337-28-9

中文名称
——
中文别名
——
英文名称
ethyl (4S,5R)-4-carbethoxy-5-phenyl-1,3,2-dioxathiolane-2-oxide
英文别名
4(S)-Phenyl-5(R)-(carboxyethyl)-1,3-dioxathiolane 2-oxide;ethyl (4R,5S)-2-oxo-5-phenyl-1,3,2-dioxathiolane-4-carboxylate
ethyl (4S,5R)-4-carbethoxy-5-phenyl-1,3,2-dioxathiolane-2-oxide化学式
CAS
172337-28-9
化学式
C11H12O5S
mdl
——
分子量
256.279
InChiKey
NUOFTBLAZNBSIG-OZZYTVELSA-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:
    373.2±42.0 °C(Predicted)
  • 密度:
    1.41±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    81
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Anchimerically assisted unprecedented SNi-type cleavage of cyclic sulfites: application in the synthesis of the calcium channel blocker diltiazem
    作者:Braj B. Lohray、Balakrishnan Jayachandran、Vidya Bhushan、Erathodiyil Nandanan、Thottappallil Ravindranathan
    DOI:10.1021/jo00123a045
    日期:1995.9
  • Asymmetric Synthesis of Tetrahydroquinolin-3-ols via CoCl<sub>2</sub>-Catalyzed Reductive Cyclization of Nitro Cyclic Sulfites with NaBH<sub>4</sub>
    作者:Arun R. Jagdale、R. Santhosh Reddy、Arumugam Sudalai
    DOI:10.1021/ol8028109
    日期:2009.2.19
    construction of chiral 3-substituted tetrahydroquinoline derivatives based on asymmetric dihydroxylation and CoCl2-catalyzed reductive cyclization of nitro cyclic sulfites with NaBH4 has been described with high optical purities. This method has been successfully applied in the formal synthesis of PNU 95666E and anachelin H chromophore.
    已经描述了具有高光学纯度的基于不对称二羟基化和CoCl 2催化的硝基环亚硫酸盐与NaBH 4的还原性环化来构建手性3-取代的四氢喹啉衍生物的新方法。该方法已成功地用于PNU 95666E和安那奇林H发色团的形式合成。
  • Nandanan; Phukan, Prodeep; Sudalai, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999, vol. 38, # 3, p. 283 - 286
    作者:Nandanan、Phukan, Prodeep、Sudalai
    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