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4-HYDROXYPHENYL BENZOATE

  • Name 4-HYDROXYPHENYL BENZOATE
  • CAS 2444-19-1
  • Purity 99%
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Product Details

Buy cost-effective 99% pure 4-HYDROXYPHENYL BENZOATE 2444-19-1 now

  • Molecular Formula: C13H10O3
  • Molecular Weight: 214.221
  • Vapor Pressure: 3.3E-06mmHg at 25°C 
  • Melting Point: 164-165 °C 
  • Refractive Index: 1.615 
  • Boiling Point: 376.6 °C at 760 mmHg 
  • PKA: 9.59±0.26(Predicted) 
  • Flash Point: 164.7 °C 
  • PSA: 46.53000 
  • Density: 1.25 g/cm3 
  • LogP: 2.61140 

4-HYDROXYPHENYL BENZOATE(Cas 2444-19-1) Usage

InChI:InChI=1/C13H10O3/c14-11-6-8-12(9-7-11)16-13(15)10-4-2-1-3-5-10/h1-9,14H

2444-19-1 Relevant articles

Nickel-catalyzed deallylation of aryl allyl ethers with hydrosilanes

Ding, Guangni,Fan, Sijie,Wang, Jingyang,Wang, Yu,Wu, Xiaoyu,Xie, Xiaomin,Yang, Liqun,Zhang, Zhaoguo

supporting information, (2021/09/28)

An efficient and mild catalytic deallyla...

N,O-Benzyl Protection of Structurally Varied Amines and Phenols Using Wells-Dawson Heteropolyacid Catalyst

Boughaba, Sara,Aouf, Zineb,Zerrouki, Rachida,Aouf, Nour Eddine

, p. 301 - 310 (2021/05/24)

-

Metal-free approach for hindered amide-bond formation with hypervalent iodine(iii) reagents: application to hindered peptide synthesis

Lee, Hyo-Jun,Huang, Xiao,Sakaki, Shigeyoshi,Maruoka, Keiji

supporting information, p. 848 - 855 (2021/02/09)

A new bio-inspired approach is reported ...

Direct hydroxylation of benzene and aromatics with H2O2 catalyzed by a self-assembled iron complex: Evidence for a metal-based mechanism

Capocasa, Giorgio,Olivo, Giorgio,Barbieri, Alessia,Lanzalunga, Osvaldo,Di Stefano, Stefano

, p. 5677 - 5686 (2017/12/07)

An iminopyridine Fe(ii) complex, easily ...

2444-19-1 Process route

(4'-benzyloxyphenyl)benzoate
2444-21-5

(4'-benzyloxyphenyl)benzoate

4-hydroxyphenyl benzoate
2444-19-1

4-hydroxyphenyl benzoate

Conditions
Conditions Yield
With cyclohexene; palladium dihydroxide; In ethanol; for 2h; Heating;
99%
With hydrogen; palladium on activated charcoal; In ethyl acetate; at 70 ℃; for 1h;
98%
palladium-carbon; In ethanol; nitrogen; hydrogen;
94%
With hydrogen; palladium on activated charcoal; In ethanol;
4-(allyloxy)phenyl benzoate
88561-74-4

4-(allyloxy)phenyl benzoate

4-hydroxyphenyl benzoate
2444-19-1

4-hydroxyphenyl benzoate

Conditions
Conditions Yield
4-(allyloxy)phenyl benzoate; With bis(1,5-cyclooctadiene)nickel (0); diphenylsilane; 4,4'-di-tert-butyl-2,2'-bipyridine; In N,N-dimethyl-formamide; at 20 ℃; for 8h; Schlenk technique; Inert atmosphere; Sealed tube;
With hydrogenchloride; In water; N,N-dimethyl-formamide; at 50 ℃; for 2h; Reagent/catalyst; Schlenk technique; Inert atmosphere; Sealed tube;
90%

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    benzoic acid phenyl ester

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    (4'-benzyloxyphenyl)benzoate

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