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7-Hydroxycoumarin-4-acetic Acid - ≥97%, high purity , CAS No.6950-82-9
Basic Description
Synonyms
7-Hydroxycoumarinyl-4-acetic acid | EN300-186397 | NSC 65625 | DTXSID50943938 | VELNACRINE [MI] | NSC642907 | NSC-642907 | 2H-1-Benzopyran-4-acetic acid, 7-hydroxy-2-oxo- | 7-Hydroxycoumarinyl-4-acetic acid, 97% | EINECS 204-249-8 | Umbelliferone-4-acetic
Specifications & Purity
≥97%
Storage Temp
Argon charged
Shipped In
Normal
Product Description
Usually used in the synthesis of novel and specific enzyme substrates for Maroteaux-Lamy (MPS VI) and Morquio A (MPS IVA) diseases, and also employed as ionic liquid matrice for MALDI-TOF MS of proteins, peptides and carbohydrates.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Coumarins and derivatives
Subclass
Hydroxycoumarins
Intermediate Tree Nodes
Not available
Direct Parent
7-hydroxycoumarins
Alternative Parents
1-benzopyrans Pyranones and derivatives 1-hydroxy-2-unsubstituted benzenoids Heteroaromatic compounds Lactones Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
7-hydroxycoumarin - Benzopyran - 1-benzopyran - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 7-hydroxycoumarins. These are coumarins that contain one or more hydroxyl groups attached to the C7 position the coumarin skeleton.
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
488195376
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488195376
IUPAC Name
2-(7-hydroxy-2-oxochromen-4-yl)acetic acid
INCHI
InChI=1S/C11H8O5/c12-7-1-2-8-6(3-10(13)14)4-11(15)16-9(8)5-7/h1-2,4-5,12H,3H2,(H,13,14)
InChIKey
BNHPMQBVNXMPDU-UHFFFAOYSA-N
Smiles
C1=CC2=C(C=C1O)OC(=O)C=C2CC(=O)O
Isomeric SMILES
C1=CC2=C(C=C1O)OC(=O)C=C2CC(=O)O
WGK Germany
3
Molecular Weight
220.18
Beilstein
204777
Reaxy-Rn
204777
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=204777&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in Methanol
Melt Point(°C)
190 °C(dec.)
Molecular Weight
220.180 g/mol
XLogP3
1.000
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
2
Exact Mass
220.037 Da
Monoisotopic Mass
220.037 Da
Topological Polar Surface Area
83.800 Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
346.000
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
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