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Chloro(chlorosulfanyl)oxomethane

Names

[ CAS No. ]:
2757-23-5

[ Name ]:
Chloro(chlorosulfanyl)oxomethane

[Synonym ]:
Carbonochloridothioic acid,anhydrosulfide with thiohypochlorous acid
MFCD00000703
EINECS 220-415-2
Chlorocarbonylsulfenyl chloride
chlorocarbonysulfenyl chloride
Chloro(chlorosulfanyl)oxomethane
Methane, chloro(chlorothio)oxo-
chlorocarbonylsulphenyl chloride
Chlorothioformyl Chloride
Chloroformylsulfenyl chloride

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
98.0±0.0 °C at 760 mmHg

[ Molecular Formula ]:
CCl2OS

[ Molecular Weight ]:
130.981

[ Flash Point ]:
53.7±22.6 °C

[ Exact Mass ]:
129.904694

[ PSA ]:
42.37000

[ LogP ]:
2.50

[ Vapour Pressure ]:
40.7±0.1 mmHg at 25°C

[ Index of Refraction ]:
1.531

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34;R36/37

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2930909090

Precursor & DownStream

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Some fluorinated heterocyclic and acyclic derivatives of chlorocarbonylsulfenyl chloride. John EO and Jean'ne MS.

J. Fluor. Chem. 36(4) , 429-38, (1987)

An improved one-pot cost-effective synthesis of N, N-disubstituted carbamoyl halides and derivatives. Adeppa K, et al.

Can. J. Chem. 88(!2) , 1277-80, (2010)

Synthesis, structure and reactivity of 5-pyranosyl-1,3,4-oxathiazol-2-ones.

Carbohydr. Res. 341(1) , 41-8, (2006)

5-(1,2,3,4-tetra-O-acetyl-alpha-D-xylopyranos-5S-C-yl)-1,3,4-oxathiazol-2-one (8) has been prepared from glucuronamide in two steps and 73% overall yield by conversion to the tetra-O-acetyl derivative...


More Articles


Related Compounds

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