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Sigma-Aldrich

3-Aminocoumarin

97%

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About This Item

Empirical Formula (Hill Notation):
C9H7NO2
CAS Number:
Molecular Weight:
161.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

135-139 °C (lit.)

SMILES string

NC1=Cc2ccccc2OC1=O

InChI

1S/C9H7NO2/c10-7-5-6-3-1-2-4-8(6)12-9(7)11/h1-5H,10H2

InChI key

QWZHDKGQKYEBKK-UHFFFAOYSA-N

Application

3-Aminocoumarin may be employed in the following studies:
  • As ligand for the synthesis of Cr(III), Ni(II), and Cu(II) complexes.
  • As starting reagent for the synthesis of 1,2,3,4-tetrahydropyrido[2,3-c]coumarins.
  • Synthesis of new 3-(heteroaryl)aminocoumarin derivatives, via optimized Buchwald-Hartwig amination reaction.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Oscar Aguilar-Sopeña et al.
International journal of molecular sciences, 21(7) (2020-04-09)
We have previously shown the delivery of phosphatase of regenerating liver-1 (PRL-1) to the immunological synapse (IS) and proposed a regulatory role of the catalytic activity of PRLs (PRL-1, PRL-2 and PRL-3) in antigen-induced IL-2 production. Nonetheless, the expression in
Iu A Vladimirov et al.
Biulleten' eksperimental'noi biologii i meditsiny, 112(10), 358-360 (1991-10-01)
The antioxidant capacity of 3-aminocoumarin, 3-oxycoumarin, 3-acetylaminocoumarin, and 3-coumarin carbonic acid has been investigated with chemiluminescence measurement and by the accumulation of TBA-active products. All coumarins were found to be antioxidants, with 3-oxy-, 3-amino- and 3-acetylamino coumarins being capable of
Abdul Amir H Kadhum et al.
Molecules (Basel, Switzerland), 16(8), 6969-6984 (2011-08-17)
3-Aminocoumarin (L) has been synthesized and used as a ligand for the formation of Cr(III), Ni(II), and Cu(II) complexes. The chemical structures were characterized using different spectroscopic methods. The elemental analyses revealed that the complexes where M=Ni(II) and Cu(II) have
Synthesis of biologically potent new 3-(heteroaryl) aminocoumarin derivatives via Buchwald-Hartwig C-N coupling.
Das AR, et al.
Tetrahedron Letters, 51(7), 1099-1102 (2010)
Wei Jia et al.
Analytica chimica acta, 957, 29-39 (2017-01-22)
An analytical method was developed and validated for simultaneous analysis of one hundred and thirty-seven veterinary drug residues and metabolites from sixteen different classes in tilapia utilizing an improved fully non-targeted way of data acquisition with fragmentation. The automated on-line

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