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About This Item
Linear Formula:
ClSO2CH2COCl
CAS Number:
Molecular Weight:
177.01
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor pressure
0.06 mmHg ( 20 °C)
Quality Level
Assay
95%
form
liquid
refractive index
n20/D 1.493 (lit.)
bp
71-72 °C/1 mmHg (lit.)
density
1.669 g/mL at 25 °C (lit.)
SMILES string
ClC(=O)CS(Cl)(=O)=O
InChI
1S/C2H2Cl2O3S/c3-2(5)1-8(4,6)7/h1H2
InChI key
MCFSNYMQISXQTF-UHFFFAOYSA-N
Application
Chlorosulfonylacetyl chloride has been used in:
- preparation of novel tricyclic benzothiazolo [2,3-c] thiadiazine antagonists of the platelet ADP receptor
- N-terminal derivatization of peptides in rapid determination of peptide or protein sequences by matrix-assisted laser desorption ionization mass spectrometry
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Supplementary Hazards
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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R M Scarborough et al.
Bioorganic & medicinal chemistry letters, 11(14), 1805-1808 (2001-07-19)
Novel non-nucleoside tricyclic platelet ADP receptor (P2Y(12)) antagonists have been discovered that bind reversibly and with high affinity to the platelet receptor. Condensation of various 2-aminobenzothiazoles with chlorosulfonylacetyl chloride affords these novel tricyclic heterocycles, which are novel and unpredicted products
T Keough et al.
Proceedings of the National Academy of Sciences of the United States of America, 96(13), 7131-7136 (1999-06-23)
A method has been developed for de novo peptide sequencing using matrix-assisted laser desorption ionization mass spectrometry. This method will facilitate biological studies that require rapid determination of peptide or protein sequences, e.g., determination of posttranslational modifications, identification of active
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