Coumarin 2

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Coumarin 2

Coumarin 2 | 26078-25-1

Catalog Number A17-0065
Category Laser Dyes
Molecular Formula C13H15NO2
Molecular Weight 217.27
Catalog Number Size Price Quantity
A17-0065 -- $--

Product Introduction

Coumarin 2 is used as an efficient laser dye for both pulsed and CW operation.

Chemical Information

Synonyms Coumarin 450; 7-(ethylamino)-4,6-dimethyl-2H-1-benzopyran-2-one
IUPAC Name 7-(ethylamino)-4,6-dimethylchromen-2-one
Canonical SMILES CCNC1=C(C=C2C(=CC(=O)OC2=C1)C)C
InChI InChI=1S/C13H15NO2/c1-4-14-11-7-12-10(5-9(11)3)8(2)6-13(15)16-12/h5-7,14H,4H2,1-3H3
InChI Key QZXAEJGHNXJTSE-UHFFFAOYSA-N
  • Product Specification
  • Application
Signal Warning
GHS Hazard Statements H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral] H312 (50%): Harmful in contact with skin [Warning Acute toxicity, dermal] H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H332 (50%): Harmful if inhaled [Warning Acute toxicity, inhalation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statement Codes P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

Coumarin 2, a versatile fluorescent dye, finds extensive utilization across diverse scientific and industrial domains. Here are four key applications of Coumarin 2:

Fluorescent Labeling: Within molecular biology and biochemistry realms, Coumarin 2 emerges as a pivotal tool for fluorescently labeling biomolecules like nucleic acids, proteins, and lipids. Its robust fluorescence properties enable the visualization and tracking of these entities within intricate biological systems. This application plays a crucial role in techniques such as fluorescence microscopy and flow cytometry, necessitating precise detection and quantification of labeled components.

Chemical Sensing: Embracing the capabilities of Coumarin 2, researchers delve into the realm of chemical sensors and biosensors, leveraging its fluorescence emission upon interaction with specific analytes. These sensors exhibit aptitude in detecting a myriad of chemical compounds, spanning ions, small molecules, and biochemical substances. By incorporating Coumarin 2 into sensor designs, scientists pave the way for sensitive and selective detection applications across environmental monitoring, medical diagnostics, and industrial quality control.

Energy Transfer Studies: Stepping into the realm of Förster Resonance Energy Transfer (FRET) studies, Coumarin 2 assumes a pivotal role in exploring biomolecular interactions. Serving as a fluorophore for either donor or acceptor roles, Coumarin 2 facilitates the measurement of distances and conformational transitions at a molecular scale. This technique plays a critical role in unraveling the intricacies of protein-protein interactions, enzyme mechanisms, and the dynamic structural attributes of nucleic acids.

Photodynamic Therapy: Delving into the realm of cancer treatment, Coumarin 2 stands out for its potential in photodynamic therapy (PDT), harnessing its ability to generate reactive oxygen species upon light activation at specific wavelengths. These reactive oxygen species are instrumental in selectively targeting and destroying cancer cells, thereby presenting a focused therapeutic solution that minimizes harm to surrounding healthy tissues. Leveraging the photochemical prowess of the dye, this application holds promise in revolutionizing targeted cancer therapies.

Computed Properties

XLogP3 2.5
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 217.110278721 g/mol
Monoisotopic Mass 217.110278721 g/mol
Topological Polar Surface Area 38.3Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 311
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

Patents

Publication NumberTitlePriority Date
CN-113666898-A Fluorescent probe for selective recognition of Hg2+ containing coumarin and preparation method thereof 2021-07-01
CN-113666898-B Fluorescent probe for selective recognition of Hg2+ containing coumarin and preparation method thereof 2021-07-01
CN-112574280-B Double-enzyme system probe and application thereof 2020-12-21
US-2022153932-A1 Prepolymers of 1,1-dicarbonyl substituted-1-alkene, methods to make them, polymers made from them and methods to make the polymer 2020-11-18
WO-2022102675-A1 Photosensitive element, method for producing cured product, method for producing cured product pattern, and method for producing wiring board 2020-11-13
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