ChemicalBook--->CAS DataBase List--->385432-46-2

385432-46-2

385432-46-2 Structure

385432-46-2 Structure
IdentificationBack Directory
[Name]

5-Benzothiazolecarbonitrile,2-chloro-(9CI)
[CAS]

385432-46-2
[Synonyms]

2-CHLORO-5-CYANOBENZOTHIAZOLE
5-Benzothiazolecarbonitrile, 2-chloro-
2-Chlorobenzo[d]thiazole-5-carbonitrile
2-chloro-1,3-benzothiazole-5-carbonitrile
5-Benzothiazolecarbonitrile,2-chloro-(9CI)
[Molecular Formula]

C8H3ClN2S
[MDL Number]

MFCD12827959
[MOL File]

385432-46-2.mol
[Molecular Weight]

194.64
Questions And AnswerBack Directory
[Uses]

2-Chlorobenzo[d]thiazole-5-carbonitrile is a useful research chemical.
Chemical PropertiesBack Directory
[Boiling point ]

336.6±15.0 °C(Predicted)
[density ]

1.51±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-1.68±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

5-Benzothiazolecarbonitrile,2-chloro-(9CI)(385432-46-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-MERCAPTO-BENZOTHIAZOLE-5-CARBONITRILE

149367-90-8

5-Benzothiazolecarbonitrile,2-chloro-(9CI)

385432-46-2

To a solution of 2-thio-2,3-dihydrobenzo[d]thiazole-5-carbonitrile (1.0 g, 5.2 mmol) in dichloromethane (10 mL) was slowly added sulfonyl chloride (13.5 g, 100 mmol) at 0 °C. The reaction mixture was then warmed to 25 °C and stirred continuously for 3 hours. Upon completion of the reaction, the mixture was poured into water (200 mL) and the dichloromethane was removed by partial vacuum concentration. The aqueous phase was extracted with ethyl acetate (3 x 90 mL) and the organic phases were combined. The organic phase was washed sequentially with brine (3 x 20 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude product was purified by silica gel column chromatography with the eluent ratio of petroleum ether:ethyl acetate=15:1 to 10:1 to afford 2-chlorobenzo[d]thiazole-5-carbonitrile (0.4 g, 40% yield) as a yellow solid.1H-NMR (CDCl3, 400MHz): δ 8.26 (d, J=0.8 Hz, 1H), 7.92 (d, J=8.4 Hz, 1H), 7.68 (d, J=8.4 Hz, 1H), 1H), 7.68 (d, J=8.4 Hz, 1H). 1H), 7.68 (dd, J=8.4, 1.6 Hz, 1H).

[References]

[1] Patent: WO2017/69980, 2017, A1. Location in patent: Paragraph 00317; 00318
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