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2-1,2,3-triphenylbutyric acid | 5468-20-2

中文名称
——
中文别名
——
英文名称
2-1,2,3-triphenylbutyric acid
英文别名
(+/-)-erythro-2.3.4-triphenyl-butyric acid;(+/-)-erythro-2.3.4-Triphenyl-buttersaeure;(2R,3S)-2,3,4-triphenylbutanoic acid
2-1,2,3-triphenylbutyric acid化学式
CAS
5468-20-2
化学式
C22H20O2
mdl
——
分子量
316.4
InChiKey
PAIMKQZXMVKNGS-RTWAWAEBSA-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

  • 熔点:
    153-154 °C
  • 沸点:
    415.6±14.0 °C(Predicted)
  • 密度:
    1.159±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.1
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:4b624cd3f7bd560e1e2aa1271f61c0e0
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-1,2,3-triphenylbutyric acid 在 potassium hydroxide 作用下, 以 乙二醇 为溶剂, 以14 g的产率得到1,2,3-triphenylbutyric acid
    参考文献:
    名称:
    Interesting Reactivity in the Thermolysis and Photolysis of 2,3-Diphenyl-1-naphthol
    摘要:
    2,3-二苯基-1-萘酚 (1) 在不同条件下发生两个意想不到的反应。化合物(1)在DMSO-d6中加热并进行Pummerer型热反应,得到两种异构产物1-(甲硫基)甲氧基-2,3-二苯基萘酚-d5,其在空间群$$ P{\bar中结晶{\text{1}}} $$,其中 a = 7.1610(9) Å、b = 11.2795(15) Å、c = 12.8905(17) Å、α = 114.049(2)°、β = 96.589(2)° ,γ = 102.945(2)°,以及 2-(甲硫基)甲基-2,3-二苯基 1(2H)-萘酮-d5,其在空间群 $$ P{\bar{\text{1}} 中结晶$$,其中 a = 8.5981(5) Å、b = 10.4374(6) Å、c = 11.1078(6) Å、α = 78.748(2)°、β = 67.709(2)° 和 γ = 83.184(2 )°。 (1) 光解 (254 nm) 生成 2,2',3,3'-四苯基-1,1'-双-2-萘酚,其在空间群 P21/c 中结晶,a = 26.3616(11) Å ,b = 10.1707(4) Å,c = 23.3376(9) Å,β = 99.034(2)°。当 2,3-二苯基-1-萘酚在 DMSO-d6 中加热时,会产生两种意想不到的异构体:1-(甲硫基)甲氧基-2,3-二苯基萘酚-d5 和外消旋体 2-(甲硫基)甲基-2,3-二苯基产生1(2H)-萘酮-d5。在 254 nm 处的 THF 中光解产生了意想不到的产物 2,2',3,3'-四苯基-1,1'-双-2-萘酚。所有结构均通过X射线晶体学阐明。
    DOI:
    10.1007/s10870-008-9491-y
  • 作为产物:
    参考文献:
    名称:
    Five- vs. Six-membered Ring Formation in the Cyclization of 2,3,4-Triphenylbutyric Acid; the Relative Importance of Stereochemistry1
    摘要:
    DOI:
    10.1021/ja01546a052
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文献信息

  • Polyphenylnaphthalenes. II. 1,2,3-Triphenylnaphthalene
    作者:Felix Bergmann、David Schapiro、H. Emile Eschinazi
    DOI:10.1021/ja01255a027
    日期:1942.3
  • Recent sediments from a coastal pond, eastern margin of the Dead Sea, Jordan
    作者:Fadhil N. Sadooni、Walid Saqqa、Ghada Abrahim
    DOI:10.1007/bf03175659
    日期:2002.3
    A marginal pond on the eastern coast of the southern part of the Dead Sea in Jordan receives fresh and thermal waters from adjacent areas. The pool has a narrow "intertidal" zone in which halite-encrusted stromatolites flourish. The muddy sediments of the pond consist of a mixture of detrital clay minerals and calcite with authigenic halite and dolomite. The association of halite with dolomite supports the assertion that dolomite is an evaporitic mineral. The absence of gypsum in these sediments is attributed to bacterial reduction of sulfates.
  • 2,3-Diphenyl-1,4-naphthoquinone<sup>1</sup>
    作者:H. Marjorie Crawford、Helen B. Nelson
    DOI:10.1021/ja01205a043
    日期:1946.1
  • Five- vs. Six-membered Ring Formation in the Cyclization of 2,3,4-Triphenylbutyric Acid; the Relative Importance of Stereochemistry<sup>1</sup>
    作者:Daniel Lednicer、Charles R. Hauser
    DOI:10.1021/ja01546a052
    日期:1958.7
  • Interesting Reactivity in the Thermolysis and Photolysis of 2,3-Diphenyl-1-naphthol
    作者:Ilia A. Guzei、Howard E. Zimmerman、Sergey Shorunov、Lara C. Spencer
    DOI:10.1007/s10870-008-9491-y
    日期:2009.6
    2,3-Diphenyl-1-naphthol (1) undergoes two unexpected reactions under different conditions. Compound (1) was heated in DMSO-d6 and underwent a Pummerer type thermal reaction to give two isomeric products, 1-(methylthio)methoxy-2,3-diphenyl naphthol-d5 which crystallized in the space group $$ P\bar\text1}}} $$ with a = 7.1610(9) Å, b = 11.2795(15) Å, c = 12.8905(17) Å, α = 114.049(2)°, β = 96.589(2)°, and γ = 102.945(2)°, and 2-(methylthio)methyl-2,3-diphenyl 1(2H)-naphthalenone-d5 which crystallized in the space group $$ P\bar\text1}}} $$ with a = 8.5981(5) Å, b = 10.4374(6) Å, c = 11.1078(6) Å, α = 78.748(2)°, β = 67.709(2)°, and γ = 83.184(2)°. Photolysis (254 nm) of (1) resulted in 2,2′,3,3′-tetraphenyl-1,1′-bi-2-naphthol which crystallized in the space group P21/c with a = 26.3616(11) Å, b = 10.1707(4) Å, c = 23.3376(9) Å, and β = 99.034(2)°. When 2,3-diphenyl-1-naphthol was heated in DMSO-d6 two unexpected isomers, 1-(methylthio)methoxy-2,3-diphenyl naphthol-d5 and the racemate 2-(methylthio)methyl-2,3-diphenyl 1(2H)-naphthalenone-d5 were produced. Photolysis in THF at 254 nm led to the unexpected product 2,2′,3,3′-tetraphenyl-1,1′-bi-2-naphthol. All structures were elucidated by X-ray crystallography.
    2,3-二苯基-1-萘酚 (1) 在不同条件下发生两个意想不到的反应。化合物(1)在DMSO-d6中加热并进行Pummerer型热反应,得到两种异构产物1-(甲硫基)甲氧基-2,3-二苯基萘酚-d5,其在空间群$$ P\bar中结晶\text1}}} $$,其中 a = 7.1610(9) Å、b = 11.2795(15) Å、c = 12.8905(17) Å、α = 114.049(2)°、β = 96.589(2)° ,γ = 102.945(2)°,以及 2-(甲硫基)甲基-2,3-二苯基 1(2H)-萘酮-d5,其在空间群 $$ P\bar\text1}} 中结晶$$,其中 a = 8.5981(5) Å、b = 10.4374(6) Å、c = 11.1078(6) Å、α = 78.748(2)°、β = 67.709(2)° 和 γ = 83.184(2 )°。 (1) 光解 (254 nm) 生成 2,2',3,3'-四苯基-1,1'-双-2-萘酚,其在空间群 P21/c 中结晶,a = 26.3616(11) Å ,b = 10.1707(4) Å,c = 23.3376(9) Å,β = 99.034(2)°。当 2,3-二苯基-1-萘酚在 DMSO-d6 中加热时,会产生两种意想不到的异构体:1-(甲硫基)甲氧基-2,3-二苯基萘酚-d5 和外消旋体 2-(甲硫基)甲基-2,3-二苯基产生1(2H)-萘酮-d5。在 254 nm 处的 THF 中光解产生了意想不到的产物 2,2',3,3'-四苯基-1,1'-双-2-萘酚。所有结构均通过X射线晶体学阐明。
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