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7-Methoxycoumarin-3-carboxylic acid - ≥97% (HPCE), high purity , CAS No.20300-59-8

COA COA
    Grade & Purity:
  • ≥97%(HPCE)
In stock
Item Number
M131451
Grouped product items
SKU Size
Availability
 Price Qty
M131451-100mg
100mg
3
$25.90
M131451-500mg
500mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$115.90
M131451-1g
1g
2
$153.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet

Amine-reactive fluorescent probe.

View related series
Six-Membered Heterocyclic Compounds (1696) Spectroscopic reagent (233)

Basic Description

Synonyms BDBM50442714 | FT-0621448 | EN300-7416483 | 7-Methoxy-2-oxo-2H-chromene-3-carboxylic acid | Cumarin-3-carboxylic acid, 7-methoxy- | HY-W039519 | SCHEMBL203997 | 7-methoxy-2-oxochromene-3-carboxylic acid | 7-Methoxy-2-oxo-2H-chromene-3-carboxylic acid # |
Specifications & Purity ≥97%(HPCE)
Biochemical and Physiological Mechanisms Amine-reactive fluorescent probe. Used for coupling to amines, hydrazines or hydroxylamines on biomolecules of interest.
Shipped In Normal
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

7-Methoxycoumarin-3-carboxylic acid provides a distinguishable contrast when used with longer-wavelength probes in certain multicolor fluorescence applications such as nucleic acid and protein microarrays, in situ hybridization and immunofluorescence.
7-Methoxycoumarin-3-carboxylic acid N-succinimidyl ester is used as a reagent to conjugate 7-Methoxycoumarin-3-carboxylic acid to other molecules via amide chemistry.

Taxonomic Classification

Taxonomy Tree

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  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Coumarin - Benzopyran - 1-benzopyran - Anisole - Alkyl aryl ether - Pyranone - Benzenoid - Pyran - Heteroaromatic compound - Lactone - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Ether - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organooxygen compound - 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

Associated Targets(Human)

MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SiHa (2051 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

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 504759364
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504759364
IUPAC Name 7-methoxy-2-oxochromene-3-carboxylic acid
INCHI InChI=1S/C11H8O5/c1-15-7-3-2-6-4-8(10(12)13)11(14)16-9(6)5-7/h2-5H,1H3,(H,12,13)
InChIKey VEEGNDSSWAOLFN-UHFFFAOYSA-N
Smiles COC1=CC2=C(C=C1)C=C(C(=O)O2)C(=O)O
Isomeric SMILES COC1=CC2=C(C=C1)C=C(C(=O)O2)C(=O)O
Molecular Weight 220.18
Reaxy-Rn 384199
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=384199&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number Certificate Type Date Item
D1720147 Certificate of Analysis Nov 16, 2022 M131451
F1821136 Certificate of Analysis Feb 16, 2022 M131451

Chemical and Physical Properties

Sensitivity Light Sensitive,Air Sensitive,Heat Sensitive
Melt Point(°C) 196 °C
Molecular Weight 220.180 g/mol
XLogP3 2.200
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 2
Exact Mass 220.037 Da
Monoisotopic Mass 220.037 Da
Topological Polar Surface Area 72.800 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

Solution Calculators

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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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