ChemicalBook--->CAS DataBase List--->2942-23-6

2942-23-6

2942-23-6 Structure

2942-23-6 Structure
IdentificationBack Directory
[Name]

2,7-Dichlorobenzothiazole
[CAS]

2942-23-6
[Synonyms]

2,7-Dichlor-benzthiazol
2,7-DICHLORO BENZOTHIAZOLE
2,7-Dichlorobenzo[d]thiazole
Benzothiazole, 2,7-dichloro-
2,7-Dichloro-1,3-benzothiazole
Benzothiazole, 2,7-dichloro- (7CI,8CI,9CI)
[Molecular Formula]

C7H3Cl2NS
[MDL Number]

MFCD09037778
[MOL File]

2942-23-6.mol
[Molecular Weight]

204.08
Chemical PropertiesBack Directory
[Boiling point ]

286.8±13.0 °C(Predicted)
[density ]

1.567±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-1.49±0.30(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[HS Code ]

29342000
Spectrum DetailBack Directory
[Spectrum Detail]

2,7-Dichlorobenzothiazole(2942-23-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2(3H)-Benzothiazolethione,7-chloro-(9CI)

1849-73-6

2,7-Dichlorobenzothiazole

2942-23-6

General procedure for the synthesis of 2,7-dichlorobenzo[d]thiazole from 7-chlorobenzo[d]thiazole-2(3H)-thione: General method: a mixture of 7-chlorobenzo[d]thiazole-2(3H)-thione (>1 g, 1 eq.) and sulfuryl chloride (10 eq.) was stirred at 20-25 °C for 15 min. Subsequently, water (2 eq.) was added and stirring was continued for 3 hours at 20-25 °C. During the reaction, the sample was removed, quenched with acetonitrile/water (2:1) and analyzed by high performance liquid chromatography (HPLC). Upon completion of the reaction, the mixture was diluted with acetonitrile (5 v/v) and the reaction was quenched by slowly adding water (20 v/v). The product precipitated from the aqueous solution and the solid was collected and washed with distilled water. Finally, the solid was dried under vacuum to give pure 2,7-dichlorobenzo[d]thiazole. For the liquid product 2-chlorobenzo[d]thiazole (13), the reaction mixture was extracted with ethyl acetate and the organic layer was dried and concentrated to give an oily product.

[References]

[1] Synthesis (Germany), 2018, vol. 50, # 10, p. 2027 - 2032
[2] Journal of Heterocyclic Chemistry, 2005, vol. 42, # 4, p. 727 - 730
[3] Gazzetta Chimica Italiana, 1965, vol. 95, p. 490 - 498
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