| Identification | More | [Name]
3-Chloro-1,2-benzisothiazole | [CAS]
7716-66-7 | [Synonyms]
3-CHLORO-1,2-BENZISOTHIAZOLE
3-CHLORO-1,2-BENZOISOTHIAZOLE
3-CHLOROBENZISOTHIAZOLE
3-CHLORO-BENZO[D]ISOTHIAZOLE
CHLOROBENZO[D]ISOTHIAZOLE
3-Chloro-1,2-Benzisonthiazole
1,2-benzisothiazole,3-(1-piperazinyl)-,monohydrochloride
2H-indole-2-one,6-choro-5-(2-chloroethyl)-1,3-dihydro
3-Choro-1,2-benzisothiazole | [EINECS(EC#)]
616-440-7 | [Molecular Formula]
C7H4ClNS | [MDL Number]
MFCD00673254 | [Molecular Weight]
169.63 | [MOL File]
7716-66-7.mol |
| Chemical Properties | Back Directory | [Appearance]
White Solid | [Melting point ]
38-39°C | [Boiling point ]
80-86°C 0,75mm | [density ]
1.435±0.06 g/cm3(Predicted) | [Fp ]
80-86°C/0.75mm | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Soluble in Chloroform, Dichloromethane and Ethyl Acetate. | [form ]
Solid | [pka]
1.05±0.50(Predicted) | [color ]
White to Low-Melting | [BRN ]
119370 | [InChI]
InChI=1S/C7H4ClNS/c8-7-5-3-1-2-4-6(5)10-9-7/h1-4H | [InChIKey]
BCPVKLRBQLRWDQ-UHFFFAOYSA-N | [SMILES]
S1C2=C(C=CC=C2)C(Cl)=N1 | [CAS DataBase Reference]
7716-66-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [Hazard Note ]
Irritant | [HS Code ]
29349990 |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
3-Chloro-1,2-benzisothiazole is used as an intermediate of Ziprasidone. | [Synthesis]
Example 1A: To a 1 L four-necked round-bottomed flask equipped with a mechanical stirrer, a thermometer and a reflux condenser tube were sequentially added 75.6 g (0.5 mol) of 1,2-benzisothiazol-3-one, 54.8 g (0.75 mol) of N,N-dimethylformamide (DMF) and 100.0 g of chlorobenzene as a solvent. Stirring was turned on and the temperature of the reaction system was maintained between 70 °C and 80 °C, followed by the slow dropwise addition of 71.4 g (0.6 mol) of thionyl chloride (SOCl2) over a period of 1 hour. After the dropwise addition was completed, the reaction mixture was kept at the same temperature and the reaction was continued with stirring for 8 hours. Upon completion of the reaction, the liquid reaction mixture was concentrated under reduced pressure to remove the solvent and unreacted thionyl chloride. The resulting crude product was subjected to decompression distillation at 128 °C under reduced pressure at 0.93 kPa to yield 75.1 g (0.45 mol) of the target product 3-chloro-1,2-benzisothiazole in 90% yield as 1,2-benzisothiazol-3-one. | [References]
[1] Patent: US5883258, 1999, A
[2] Patent: US2013/5983, 2013, A1. Location in patent: Page/Page column 2-3
[3] Patent: US5883258, 1999, A
[4] Tetrahedron Letters, 2011, vol. 52, # 50, p. 6775 - 6778
[5] Journal of Medicinal Chemistry, 1986, vol. 29, # 3, p. 359 - 369 |
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