Catalyst and Auxiliary

131-56-6

  • Product Name:2,4-Dihydroxybenzophenone
  • Molecular Formula:C13H10O3
  • Specifications:99%
  • Molecular Weight:214.221
Inquiry

Product Details;

CasNo: 131-56-6

Molecular Formula: C13H10O3

Appearance: yellow crystalline powder

Purity 99% Min 2,4-Dihydroxybenzophenone 131-56-6 Spot Supply with Safe Transportation

  • Molecular Formula:C13H10O3
  • Molecular Weight:214.221
  • Appearance/Colour:yellow crystalline powder 
  • Vapor Pressure:2.84E-07mmHg at 25°C 
  • Melting Point:144.5-147 °C(lit.) 
  • Refractive Index:1.647 
  • Boiling Point:409 °C at 760 mmHg 
  • PKA:7.72±0.35(Predicted) 
  • Flash Point:215.3 °C 
  • PSA:57.53000 
  • Density:1.302 g/cm3 
  • LogP:2.32880 

2,4-Dihydroxybenzophenone(Cas 131-56-6) Usage

Preparation

Obtained by condensation of benzanilide with resorcinol in the presence of zinc chloride and phosphorous oxychloride at 130–140° for 1 h (25%).

Contact allergens

BZP-1 is used, for example, in paints, plastics, and nail varnishes.

Safety Profile

Poison by intravenous and intraperitoneal routes. Mildly toxic by ingestion. An eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Recrystallise it from MeOH. [Beilstein 8 IV 2442.]

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

131-56-6 Relevant articles

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, p. 1558 - 1563 (2017)

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Disclosed herein are the synthesis of ne...

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131-56-6 Process route

benzoic acid anhydride
93-97-0

benzoic acid anhydride

recorcinol
108-46-3

recorcinol

2.4-dihydroxybenzophenone
131-56-6

2.4-dihydroxybenzophenone

Conditions
Conditions Yield
With 5% CeO2 doped HZSM-5 zeolite; In ethanol; at 73 ℃; for 4h; Concentration; Reagent/catalyst; Green chemistry;
96.58%
With sulfuric acid; at 130 ℃;
 
benzoic acid
65-85-0,8013-63-6

benzoic acid

recorcinol
108-46-3

recorcinol

2.4-dihydroxybenzophenone
131-56-6

2.4-dihydroxybenzophenone

Conditions
Conditions Yield
With phosphotungstic acid; In 5,5-dimethyl-1,3-cyclohexadiene; at 130 ℃; for 5h; Temperature; Catalytic behavior;
99%
With aluminum oxide; methanesulfonic acid; at 140 ℃; for 0.5h;
85%
With bismuth(lll) trifluoromethanesulfonate; In neat (no solvent); at 180 ℃; for 0.5h; chemoselective reaction; Microwave irradiation;
85%
With methanesulfonic acid; pyrographite; at 120 ℃; for 2.5h;
80%
benzoic acid; With trifluoromethylsulfonic anhydride; In nitromethane; at 20 - 60 ℃;
recorcinol; In nitromethane; at 60 ℃; for 0.0833333h; regiospecific reaction;
74%
With phosphorus pentoxide; silica gel; at 100 ℃; for 24h;
66%
With boron trifluoride; at 160 ℃;
 
With zinc(II) chloride;
 
With zinc(II) chloride; at 160 ℃;
 
boron trifluoride diethyl etherate; at 95 ℃; for 2h;
 
With sulfolane; aluminum (III) chloride; at 65 - 70 ℃; for 8h;
 
With zinc(II) chloride; trichlorophosphate; at 65 ℃; for 6h; Reagent/catalyst; Temperature;
8.7 g
With sodium montmorillonite; In 5,5-dimethyl-1,3-cyclohexadiene; at 150 ℃; for 8h;
46.13 g

131-56-6 Upstream products

  • 3555-84-8
    3555-84-8

    2,4-dimethoxybenzophenone

  • 101894-07-9
    101894-07-9

    (2,4-Dihydroxy-phenyl)-diphenyl-methanol

  • 55-21-0
    55-21-0

    benzamide

  • 108-46-3
    108-46-3

    recorcinol

131-56-6 Downstream products

  • 101293-72-5
    101293-72-5

    5-dimethylaminomethyl-2,4-dihydroxy-benzophenone; hydrochloride

  • 102178-02-9
    102178-02-9

    2,4-dihydroxy-5-piperidinomethyl-benzophenone; hydrochloride

  • 101894-07-9
    101894-07-9

    (2,4-Dihydroxy-phenyl)-diphenyl-methanol

  • 3286-96-2
    3286-96-2

    3,5-Dibrom-2,4-dihydroxy-benzophenon

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