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Merck
CN

417351

4-Hydroxy-6-methylcoumarin

98%

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About This Item

Empirical Formula (Hill Notation):
C10H8O3
CAS Number:
Molecular Weight:
176.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
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assay

98%

mp

261-264 °C (lit.)

functional group

ester, ketone

SMILES string

Cc1ccc2OC(=O)C=C(O)c2c1

InChI

1S/C10H8O3/c1-6-2-3-9-7(4-6)8(11)5-10(12)13-9/h2-5,11H,1H3

InChI key

WIRGBZBGYNIZIB-UHFFFAOYSA-N

Application

4-Hydroxy-6-methylcoumarin may be used for the in situ generation of α-methylenechromanes, α-methylenequinoline and ortho-quinone methides, via Knoevenagel reaction. It may be used for the preparation of 8-methyl-2-phenyl-4H-furo-[3,2-c]benzopyran-4-one and 6-methyl-2-phenyl-4H-furo-[2,3-b]benzopyran-4-one.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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Efficient One-Step Synthesis of 2-AryI furans by Ceric Ammonium Nitrate (CAN)-Mediated Cycloaddition of 1, 3-Dicarbonyl Compounds to Alkynes.
Lee YR, et al.
Bull. Korean Chem. Soc., 19(10), 1081-1081 (1998)
José C J M D S Menezes et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(42), 13644-13655 (2014-08-30)
In view of increasing demands for efficient photosensitizers for photodynamic therapy (PDT), we herein report the synthesis and photophysical characterizations of new chlorin e6 trimethyl ester and protoporphyrin IX dimethyl ester dyads as free bases and Zn(II) complexes. The synthesis of these
Jin Kyu Kang et al.
Molecules (Basel, Switzerland), 25(19) (2020-10-01)
Coumarins are natural products with promising pharmacological activities owing to their anti-inflammatory, antioxidant, antiviral, anti-diabetic, and antimicrobial effects. Coumarins are present in many plants and microorganisms and have been widely used as complementary and alternative medicines. To date, the pharmacological



Global Trade Item Number

SKUGTIN
417351-1G04061826663257