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2-CHLORO-1,4-BENZOQUINONE

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2-CHLORO-1,4-BENZOQUINONE Basic information

Product Name:
2-CHLORO-1,4-BENZOQUINONE
Synonyms:
  • 2-CHLORO-1,4-BENZOQUINONE
  • benzoquinone,2-chloro-
  • Chloro-1,4-benzoquinone
  • Chloro-p-benzoquinone
  • Chloroquinone
  • Monochloro-p-benzoquinone
  • Monochloroquinone
  • p-Benzoquinone, 2-chloro-
CAS:
695-99-8
MF:
C6H3ClO2
MW:
142.54
Product Categories:
  • C3 to C6
  • Carbonyl Compounds
  • Ketones
Mol File:
695-99-8.mol
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2-CHLORO-1,4-BENZOQUINONE Chemical Properties

Melting point:
52-57 °C
Boiling point:
210℃
Density 
1.40
refractive index 
1.4620 (estimate)
Flash point:
83℃
storage temp. 
Storage temp. 2-8°C
form 
Crystals
color 
Yellow to brown
CAS DataBase Reference
695-99-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn,F
Risk Statements 
36/37/38-15-10
Safety Statements 
26-37/39-43-36-7/8
WGK Germany 
3
HS Code 
29147000

MSDS

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2-CHLORO-1,4-BENZOQUINONE Usage And Synthesis

Chemical Properties

YELLOW TO BROWN CRYSTALS

Uses

2-Chloro-1,4-benzoquinone may be used in the preparation of chloro derivatives of prenylnaphthohydroquinone.

General Description

2-Chloro-1,4-benzoquinone is a quinone derivative. It is one of the intermediate formed during the degradation of 3,4-dichloroaniline in a dielectric barrier discharge plasma reactor. It is formed during lignin peroxidase catalyzed oxidation of 2-chloro-1,4-dimethoxybenzene. 2-Chloro-1,4-benzoquinone on dechlorination yields 1,2,4-trihydroxybenzene.

Synthesis

609-66-5

695-99-8

GENERAL METHOD: Diacetoxyiodobenzene (5 mmol, 1.61 g) and NaHSO4-H2O (1 mmol, 0.138 g) were stirred in an aqueous acetonitrile solution (5 mL of water and 5 mL of acetonitrile) for 10-15 minutes at room temperature. To this reaction mixture, 2-chlorobenzamide (1 mmol) was added and stirring was continued until the reaction was complete (monitored by TLC). Upon completion of the reaction, the reaction mixture was quenched with ice water and subsequently extracted with chloroform (3 x 10 mL). The chloroform layers were combined, washed with water (3 x 20 mL), dried with anhydrous Na2SO4 and concentrated on a rotary evaporator to give the crude product. The crude product was further purified by silica gel column chromatography using ethyl acetate: hexane (1:9, v/v) as eluent to give pure 2-chloro-1,4-benzoquinone.

References

[1] Organic Letters, 2010, vol. 12, # 20, p. 4644 - 4647
[2] Synthetic Communications, 2014, vol. 44, # 4, p. 468 - 473

2-CHLORO-1,4-BENZOQUINONE Preparation Products And Raw materials

Preparation Products

2-CHLORO-1,4-BENZOQUINONESupplier

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