837-08-1 (2,4'-异亚丙基二苯酚,2,4'-Bisphenol A)

CAS号:
837-08-1
中文名称:
2,4'-异亚丙基二苯酚
英文名称:
2,4'-Bisphenol A
分子式:
C15H16O2
分子量:
228.286344528198

2,4'-异亚丙基二苯酚(837-08-1)名称与标识符

名称

中文别名:
2,4'-异亚丙基二苯酚;
英文别名:
Phenol,2-[1-(4-hydroxyphenyl)-1-methylethyl]-;2,4'-BISPHENOL A;2-[2-(4-hydroxyphenyl)propan-2-yl]phenol;o-[1-(4-hydroxyphenyl)-1-methylethyl]phenol;2-[1-(4-Hydroxyphenyl)-1-methylethyl]phenol (ACI);Phenol, 2,4′-isopropylidenedi- (8CI);2,4′-Bisphenol A;2,4′-Dihydroxydiphenyldimethylmethane;2,4′-Isopropylidenebisphenol;2,4′-Isopropylidenediphenol;2-(2-Hydroxyphenyl)-2-(4-hydroxyphenyl)propane;4-[2-(2-Hydroxyphenyl)-2-propyl]phenol;o,p-Diphenylolpropane;o,p′-Bisphenol A;o,p′-Dian;2-(2-(4-Hydroxyphenyl)propan-2-yl)phenol;2,4'-(propane-2,2-diyl)diphenol;Phenol, 2-(1-(4-hydroxyphenyl)-1-methylethyl)-;2,4'-Dihydroxydiphenyldimethylmethane;NS00019384;2,4'-Isopropylidenediphenol;o,p'-bisphenol;2,4-Bisphenol A;4-(2-(2-HYDROXYPHENYL)-2-PROPYL) PHENOL;EINECS 212-650-4;2,4-D IAN;4-[2-(2-HYDROXYPHENYL)PROPAN-2-YL]PHENOL;UNII-43OH5D3Y72;AKOS028110997;Oprea1_000789;SCHEMBL177979;DTXSID7042275;2-[1-(4-hydroxyphenyl)-1-methylethyl]phenol;2,4'-isopropylidenebisphenol;Phenol, 2-[1-(4-hydroxyphenyl)-1-methylethyl]-;43OH5D3Y72;2-(4'-Hydroxyphenyl)-2-(2'-hydroxyphenyl)propane;Phenol, 2,4'-isopropylidenedi-;2-(4'-Hydroxyphenyl)2-(2'-hydroxyphenyl)propane;Q27258662;837-08-1;o-(1-(4-Hydroxyphenyl)-1-methylethyl)phenol;G68639;

标识符

InChIKey:
MLCQXUZZAXKTSG-UHFFFAOYSA-N
Inchi:
1S/C15H16O2/c1-15(2,11-7-9-12(16)10-8-11)13-5-3-4-6-14(13)17/h3-10,16-17H,1-2H3
SMILES:
OC1C=CC(C(C)(C)C2C(O)=CC=CC=2)=CC=1

2,4'-异亚丙基二苯酚(837-08-1)物化性质

计算特性

  • 精确分子量 : 228.115029749g/mol
  • 氢键供体数量 : 2
  • 氢键受体数量 : 2
  • 可旋转化学键数量 : 2
  • 同位素质量 : 228.115029749g/mol
  • 重原子数量 : 17
  • 复杂度 : 241
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 4.1
  • 拓扑分子极性表面积 : 40.5Ų

2,4'-异亚丙基二苯酚(837-08-1)合成路线

合成路线:1 步
反应条件:
参考文献:
Reaction of phenol with acetone in the presence of aluminum phenolate
Kozlikovskii, Ya. B.; et al, Zhurnal Organicheskoi Khimii, 1985, 21(3), 565-8
合成路线:1 步
反应条件:
参考文献:
Reaction of phenol with acetone in the presence of aluminum phenolate
Kozlikovskii, Ya. B.; et al, Zhurnal Organicheskoi Khimii, 1985, 21(3), 565-8
合成路线:1 步
反应条件:
参考文献:
Preparation of bisphenol A by the condensation of phenol and acetone in the presence of acid catalyst and additives
, European Patent Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Enhanced cooperative, catalytic behavior of organic functional groups by immobilization
Zeidan, Ryan K.; et al, Journal of Catalysis, 2006, 239(2), 299-306
合成路线:1 步
反应条件:
参考文献:
Estrogenic Activity of Impurities in Industrial Grade Bisphenol A
Terasaki, Masanori; et al, Environmental Science and Technology, 2005, 39(10), 3703-3707
合成路线:2 步
反应条件:
参考文献:
Estrogenic Activity of Impurities in Industrial Grade Bisphenol A
Terasaki, Masanori; et al, Environmental Science and Technology, 2005, 39(10), 3703-3707
合成路线:1 步
反应条件:
参考文献:
Synthesis of bisphenol A catalyzed by H2SO4-SiO2 solid acid
Hou, Lijie; et al, Gongye Cuihua, 2008, 16(12), 68-71
合成路线:1 步
反应条件:
参考文献:
Preparation of bisphenol-A zeolite catalysts
Singh, A. P., Catalysis Letters, 1992, 16(4), 431-5
合成路线:1 步
反应条件:
参考文献:
Oligomeric hydroxy-aryloxy phosphazene based on cyclic chlorophosphazenes
Sirotin, I. S.; et al, Russian Journal of Applied Chemistry, 2013, 86(12), 1903-1912