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Assay
97%
mp
300-304 °C (lit.)
SMILES string
CC1=C(C#N)C(=O)Oc2cc(O)ccc12
InChI
1S/C11H7NO3/c1-6-8-3-2-7(13)4-10(8)15-11(14)9(6)5-12/h2-4,13H,1H3
InChI key
GLGBPOSQDAZSIZ-UHFFFAOYSA-N
Related Categories
General description
3-Cyano-7-hydroxy-4-methylcoumarin has been isolated from Curcuma longa isopropanol extract.
Application
3-Cyano-7-hydroxy-4-methylcoumarin (CHMC) may be used as reagent for the stereo-specific preparation of RP- and SP-O-alkyl methylphosphonyl-CHMC esters.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Evidence-based complementary and alternative medicine : eCAM, 2011, doi:10-doi:10 (2010-10-19)
Pancreatic α-amylase inhibitors offer an effective strategy to lower the levels of post prandial hyperglycemia via control of starch breakdown. Eleven Ayurvedic Indian medicinal plants with known hypoglycemic properties were subjected to sequential solvent extraction and tested for α-amylase inhibition
Chemico-biological interactions, 187(1-3), 362-369 (2010-03-23)
Fluorogenic organophosphate inhibitors of acetylcholinesterase (AChE) homologous in structure to nerve agents provide useful probes for high throughput screening of mammalian paraoxonase (PON1) libraries generated by directed evolution of an engineered PON1 variant with wild-type like specificity (rePON1). Wt PON1
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