4,6-DIACETYLRESORCINOL

4,6-DIACETYLRESORCINOL Structure
CAS No.
2161-85-5
Chemical Name:
4,6-DIACETYLRESORCINOL
Synonyms
AKOS 236-35;RESODIACETOPHENONE;4,6-DIACETYLRESORCINOL;2,4-Diacetyl-1,5-benzenediol;4,6-Diacetyl-1,3-dihydroxybenzene;1,1'-(4,6-Dihydroxy-1,3-phenylene);5'-Acetyl-2',4'-dihydroxyacetophenone;1-(5-acetyl-2,4-dihydroxyphenyl)ethanone;1-(5-ACETYL-2,4-DIHYDROXYPHENYL)ETHAN-1-ONE;1,1'-(4,6-Dihydroxy-1,3-phenylene)diethanone
CBNumber:
CB7329353
Molecular Formula:
C10H10O4
Molecular Weight:
194.18
MOL File:
2161-85-5.mol
MSDS File:
SDS
Modify Date:
2023/6/8 17:06:37

4,6-DIACETYLRESORCINOL Properties

Melting point 178-180 °C(lit.)
Boiling point 399.9±27.0 °C(Predicted)
Density 1.300±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka 7.87±0.23(Predicted)
form Crystalline Powder
color White to off-white
λmax 370nm(DMF)(lit.)
CAS DataBase Reference 2161-85-5(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352+P312-P304+P340+P312-P305+P351+P338
Hazard Codes  Xn
Risk Statements  20/21/22-36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29145090
NFPA 704
0
2 0

4,6-DIACETYLRESORCINOL price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 391794 1,1′-(4,6-Dihydroxy-1,3-phenylene)bisethanone 99% 2161-85-5 5G ₹7274.4 2022-06-14 Buy
TCI Chemicals (India) D5102 4,6-Diacetylresorcinol min. 98.0 % 2161-85-5 5G ₹6800 2022-05-26 Buy
Product number Packaging Price Buy
391794 5G ₹7274.4 Buy
D5102 5G ₹6800 Buy

4,6-DIACETYLRESORCINOL Chemical Properties,Uses,Production

Chemical Properties

Off-white powder

Uses

1,1′-(4,6-Dihydroxy-1,3-phenylene)bisethanone (4,6-diacetylresorcinol, DAR) may be used in the synthesis of the following:

  • Schiff base ligands
  • hexadentate chalcogenated bisimine ligands
  • 1,5-benzodiazepines
  • ketimine of chitosan
  • mannich bases
  • hydrazone ligands
  • thiosemicarbazone, semicarbazone and thiocarbohydrazone ligands
  • binuclear cobalt(II) and copper(II) complexes
  • europium (III) complexes

Preparation

Preparation by Friedel–Crafts acylation of resorcinol,
? with acetic anhydride,
– in the presence of zinc chloride
at 142–150° for 15 min (96%) or at 150–160° for 20 min (68%)
; – in the presence of ferric chloride
. – in the presence of concentrated sulfuric acid at 130° for 15 min (15%)
; – in the presence of 70% perchloric acid at 125–135° for 15–20 min (42%)
. ? with acetyl chloride,
– in the presence of zinc chloride, at 120°
; – in the presence of ferric chloride, at 150° for 15 min (60%) or at reflux for 30 min
; – in the presence of concentrated sulfuric acid (18%)
. ? by a typical Friedel–Crafts reaction (24%).

General Description

1,1′-(4,6-Dihydroxy-1,3-phenylene)bisethanone (4,6-diacetylresorcinol, DAR) is a bifunctional carbonyl compound. Its synthesis by acetylating resorcinol in the presence of zinc chloride has been reported. The crystal structure of DAR has been studied.

4,6-DIACETYLRESORCINOL Preparation Products And Raw materials

Raw materials

Preparation Products

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Ethanone, 1,1'-(4,6-dihydroxy-1,3-phenylene)bis- 4,6-DIACETYLRESORCINOL AKOS 236-35 1,1'-(4,6-DIHYDROXY-1,3-PHENYLENE)BISETHANONE 1,1'-(4,6-dihydroxy-1,3-phenylene)bisethan-1-one 1-(5-ACETYL-2,4-DIHYDROXYPHENYL)ETHAN-1-ONE RESODIACETOPHENONE 1,1'-(4,6-Dihydroxy-1,3-phenylene)bisethanone 99% 1,1'-(4,6-Dihydroxy-1,3-phenylene) 2,4-Diacetyl-1,5-benzenediol 5'-Acetyl-2',4'-dihydroxyacetophenone 1,1'-(4,6-Dihydroxy-1,3-phenylene)bisethanone,99% 4,6-Diacetyl-1,3-dihydroxybenzene 1,1'-(4,6-Dihydroxy-1,3-phenylene)diethanone JRH-01015, 1,1'-(4,6-Dihydroxy-1,3-phenylene)bisethanone, 97% 1-(5-acetyl-2,4-dihydroxyphenyl)ethanone 1,1'-(4,6-Dihydroxy-1,3-phenylene)diethanone 2161-85-5 HO2C6H2COCH32 Organic Building Blocks Ketones Carbonyl Compounds Building Blocks C10 Aromatic Acetophenones & Derivatives (substituted) Building Blocks C10 Carbonyl Compounds Chemical Synthesis Ketones Organic Building Blocks