2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide

Modify Date: 2024-01-10 20:06:21

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide Structure
2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide structure
Common Name 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide
CAS Number 14070-51-0 Molecular Weight 217.630
Density 1.8±0.1 g/cm3 Boiling Point 388.6±25.0 °C at 760 mmHg
Molecular Formula C7H4ClNO3S Melting Point 148-152ºC(lit.)
MSDS Chinese USA Flash Point 188.8±23.2 °C
Symbol GHS07 GHS08
GHS07, GHS08
Signal Word Warning

 Names

Name 2-chloro-1,1-dioxo-1,2-benzothiazol-3-one
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.8±0.1 g/cm3
Boiling Point 388.6±25.0 °C at 760 mmHg
Melting Point 148-152ºC(lit.)
Molecular Formula C7H4ClNO3S
Molecular Weight 217.630
Flash Point 188.8±23.2 °C
Exact Mass 216.960037
PSA 62.83000
LogP 1.22
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.693
Storage condition 2-8°C

 Safety Information

Symbol GHS07 GHS08
GHS07, GHS08
Signal Word Warning
Hazard Statements H302-H312-H332-H351
Precautionary Statements P280
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn: Harmful;
Risk Phrases 20/21/22-40
Safety Phrases 22-26-36/37/39
RIDADR NONH for all modes of transport
HS Code 2934100090

 Customs

HS Code 2934100090
Summary 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 Articles3

More Articles
N-chlorosaccharin as a possible chlorinating reagent: structure, chlorine potential, and stability in water and organic solvents.

J. Pharm. Sci. 59(7) , 955-9, (1970)

Titrimetric determination of iodine-bromine numbers of some edible oils using three N-chloroimides.

J. Assoc. Off. Anal. Chem. 70(4) , 762-3, (1987)

Three simple titrimetric methods have been developed to determine iodine-bromine numbers of some edible oils, such as coconut, gingelly, groundnut, mustard, olive, palm olein, and sunflower, using 3 N...

Ritter-type reactions of N-chlorosaccharin: a method for the electrophilic diamination of alkenes.

Org. Lett. 5(18) , 3313-5, (2003)

[reaction: see text] N-Chlorosaccharin has been shown to undergo electrophilic Ritter-type reactions with alkenes in acetonitrile. The resulting labile beta-chloro sulfonylamidines can be ring-opened ...

 Synonyms

1,2-Benzisothiazol-3(2H)-one, 2-chloro-, 1,1-dioxide
2-chlorobenzo-1,2-thiazolin-3-one-1,1-dioxide
2-Chloro-1,2-benzothiazol-3(2H)-one 1,1-dioxide
N-Chlorosaccharin
MFCD00274277