7-Amino-4-chloromethylcoumarin

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7-Amino-4-chloromethylcoumarin

7-Amino-4-chloromethylcoumarin | CAS 147963-22-2

Catalog Number A16-0077
Category Cell Proliferation Tracer Fluorescent Probes
Molecular Formula C10H8NO2Cl
Molecular Weight 209.63
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Product Introduction

7-Amino-4-chloromethylcoumarin is a coumarin-based fluorophore known for its blue fluorescence emission, which is often utilized in biochemical labeling and imaging applications. This compound contains a chloromethyl group that can react with nucleophilic sites on biomolecules, enabling covalent attachment and subsequent fluorescent tagging of proteins or other macromolecules. Its photophysical properties, including excitation and emission spectra, make it suitable for use in fluorescence microscopy and flow cytometry, where it functions as a reporter molecule to track and visualize biological processes.

  • Chemical Information

  • Application

  • Computed Properties

  • Literatures

  • Patents

Chemical Information

Synonyms CellHunt Blue CMAC; 7-amino-4-(chloromethyl)-2H-chromen-2-one; 7-amino-4-(chloromethyl)chromen-2-one
IUPAC Name 7-amino-4-(chloromethyl)chromen-2-one
SMILES C1=CC2=C(C=C1N)OC(=O)C=C2CCl
InChI InChI=1S/C10H8ClNO2/c11-5-6-3-10(13)14-9-4-7(12)1-2-8(6)9/h1-4H,5,12H2
InChIKey VIEYMVWPECAOCY-UHFFFAOYSA-N

Application

Computed Properties

Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 1
Exact Mass 209.0243562 g/mol
Monoisotopic Mass 209.0243562 g/mol
Topological Polar Surface Area 52.3Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 277
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

Literatures

PMID Publication Date Title Journal
20162389 2011-01-01 Wallerian-like degeneration of central neurons after synchronized and geometrically registered mass axotomy in a three-compartmental microfluidic chip Neurotoxicity research
21765948 2011-01-01 Calpain and PARP activation during photoreceptor cell death in P23H and S334ter rhodopsin mutant rats PloS one
21184674 2010-12-24 Tetherin restricts direct cell-to-cell infection of HIV-1 Retrovirology
21049044 2010-10-25 Moderation of calpain activity promotes neovascular integration and lumen formation during VEGF-induced pathological angiogenesis PloS one
19114102 2009-04-01 Spitzenkörper, vacuoles, ring-like structures, and mitochondria of Phanerochaete velutina hyphal tips visualized with carboxy-DFFDA, CMAC and DiOC6(3) Mycological research

Patents

Publication Number Title Priority Date
WO-2022240655-A1 Methods of using shaped particles in flow cytometers for assays on b cells and t cells 2021-05-10
EP-4071148-A1 Dichalcogenide prodrugs 2021-04-07
WO-2022214598-A1 Dichalcogenide prodrugs 2021-04-07
EP-4062942-A1 Disulfide-based prodrug compounds 2021-03-22
WO-2022200347-A1 Disulfide-based prodrug compounds 2021-03-22

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