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3,4-Dichloroisocoumarin_Molecular_structure_CAS_51050-59-0)
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3,4-Dichloroisocoumarin

Catalog No. 35913 Name Sigma Aldrich
CAS Number 51050-59-0 Website http://www.sigmaaldrich.com
M. F. C9H4Cl2O2 Telephone 1-800-521-8956
M. W. 215.03286 Fax
Purity ≥99.0% (TLC) Email
Storage Chembase ID: 4039

SYNONYMS

IUPAC name
3,4-dichloro-1H-isochromen-1-one
IUPAC Traditional name
3,4-dichloroisocoumarin
Synonyms
3,4-DCI
3,4-Dichloro-2-benzopyran-1-one

DATABASE IDS

MDL Number MFCD00036960
Beilstein Number 6802625
CAS Number 51050-59-0

PROPERTIES

Empirical Formula (Hill Notation) C9H4Cl2O2
Purity ≥99.0% (TLC)
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H315-H319-H335
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements P261-P301 + P310-P305 + P351 + P338
RID/ADR UN 2811 6.1/PG 3
Risk Statements 25-36/37/38
Safety Statements 26-36
Storage Temperature 2-8°C
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Other Notes
Effective concentration 5-100 μM.
Inhibitor of serine proteases1; Inhibition of porcine pancreatic elastase2
Quantity
Half-life = 20 min at pH 7.5.
Substrates
Serine protease inhibitor. Active towards a wide range of serine proteases including granzymes. Not active toward β-lactamases.
Biochem/physiol Actions
Inhibitor of serine proteases1 and porcine pancreatic elastase2. Treatment of proteasomes leads to rapid inactivation of chymotrypsin-like activity and slower inactivation of other proteases.3
Description (简体中文)
Other Notes
Effective concentration 5-100 μM.
Inhibitor of serine proteases1; Inhibition of porcine pancreatic elastase2
Quantity
Half-life = 20 min at pH 7.5.
Substrates
Serine protease inhibitor. Active towards a wide range of serine proteases including granzymes. Not active toward β-lactamases.
Biochem/physiol Actions
Inhibitor of serine proteases1 and porcine pancreatic elastase2. Treatment of proteasomes leads to rapid inactivation of chymotrypsin-like activity and slower inactivation of other proteases.3

REFERENCES