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5,7-Dimethoxycoumarin - 98%, high purity , CAS No.487-06-9
Basic Description
Synonyms
5,7-Dimethyloxy-2H-1-benzopyran-2-one | CAS-487-06-9 | COUMARIN, 5,7-DIMETHOXY- | NXJCRELRQHZBQA-UHFFFAOYSA-N | AI3-36094 | AQ-358/43417403 | CCG-40277 | SPBio_000707 | HY-N7085 | KBio2_003291 | MFCD00006870 | NINDS_000391 | NSC217987 | NSC-217987 | 2H-1-
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
5,7-Dimethoxycoumarin induces the processes of differentiation and melanogenesis in murine (B16) and human (A375)
Shipped In
Normal
Product Description
Product description:
5,7-dimethoxycoumarin is isolated and identified from leaves and fruits of Pelea anisata H. Mann, a plant whose fruit are used in the construction of mohikana leis. It induces frameshift mutagenesis in bacteria. It also causes lethal photosensitization and the formation of sister chromatid exchanges in Chinese hamster cells.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Coumarins and derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Coumarins and derivatives
Alternative Parents
1-benzopyrans Anisoles Pyranones and derivatives Alkyl aryl ethers Heteroaromatic compounds Lactones Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Coumarin - Benzopyran - 1-benzopyran - Anisole - Alkyl aryl ether - Pyranone - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Oxacycle - Ether - Organoheterocyclic compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488179723
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488179723
IUPAC Name
5,7-dimethoxychromen-2-one
INCHI
InChI=1S/C11H10O4/c1-13-7-5-9(14-2)8-3-4-11(12)15-10(8)6-7/h3-6H,1-2H3
InChIKey
NXJCRELRQHZBQA-UHFFFAOYSA-N
Smiles
COC1=CC2=C(C=CC(=O)O2)C(=C1)OC
Isomeric SMILES
COC1=CC2=C(C=CC(=O)O2)C(=C1)OC
WGK Germany
3
Molecular Weight
206.19
Reaxy-Rn
187066
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=187066&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Melt Point(°C)
146-149°C
Molecular Weight
206.190 g/mol
XLogP3
1.900
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
2
Exact Mass
206.058 Da
Monoisotopic Mass
206.058 Da
Topological Polar Surface Area
44.800 Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
274.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Suo Lili, Hu Meihua.
(2023)
One-Step Synthesis of Polydopamine-Coated Dummy Molecularly Imprinted Polymers on the Surface of Fe3O4 for Selective Extraction and Enrichment of Aflatoxin B in Foods Prior to High-Performance Liquid Chromatography Detection.
JOURNAL OF ANALYTICAL CHEMISTRY,
78
(2):
(213-221).
2.
Xiaopeng Hu, Ke Wang, Yufan Yang, Baomiao Ding, Chunqi Yu.
(2025)
Fluorescence/colorimetric sensor based on aptamers-molecular imprinted polymers synergistic recognition for ultrasensitive and interference-free detection of aflatoxin B1.
FOOD CHEMISTRY,
467
(142387).
3.
Li-Hong Su, Hai-Long Qian, Cheng Yang, Chuanxi Wang, Zhenyu Wang, Xiu-Ping Yan.
(2024)
Integrating molecular imprinting into flexible covalent organic frameworks for selective recognition and efficient extraction of aflatoxins.
JOURNAL OF HAZARDOUS MATERIALS,
467
(133755).
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