63989-79-7

Basic information

• Product Name: 6-AMINOCOUMARIN HYDROCHLORIDE
• Synonyms: 6-AMINOCOUMARIN HYDROCHLORIDE;6-AMINO-1,2-BENZOPYRONE HYDROCHLORIDE;6-amino-coumarihydrochloride;6-Coumarinamine hydrochloride;6-AminocoumarinHcl;6-Aminocoumarinhydrochloride,97%;6-Aminocoumarine Hydrochloride;(2-oxochromen-6-yl)azanium chloride
• CAS NO: 63989-79-7
• Molecular Formula: C₉H₇NO₂*ClH
• Molecular Weight: 197.62
• Product Categories: Coumarins
• Mol File: 63989-79-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: >260°C (dec.)
• Boiling Point: 396.9°Cat760mmHg
• Flash Point: 231°C
• Appearance: /
• Density: g/cm³
• Water Solubility: Insoluble in water.
• BRN: 3698955
• CAS DataBase Reference: 6-AMINOCOUMARIN HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINOCOUMARIN HYDROCHLORIDE(63989-79-7)
• EPA Substance Registry System: 6-AMINOCOUMARIN HYDROCHLORIDE(63989-79-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38-20/21/22-36
• Safety Statements: 22-36/37-36-26
• RTECS: GN4930000
• Hazardous Substances Data: 63989-79-7(Hazardous Substances Data)

Usage

Description

6-Aminocoumarin hydrochloride is an organic compound that exists as a pale brown or yellow solid. It is a derivative of coumarin, which is a type of organic compound that has a wide range of applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
6-Aminocoumarin hydrochloride is used as a pharmaceutical intermediate for the synthesis of various drugs. Its chemical structure allows it to be a key component in the development of medications that target specific biological pathways or receptors.
Used in Chemical Synthesis:
6-Aminocoumarin hydrochloride serves as a building block in the synthesis of other organic compounds, particularly those with potential applications in the pharmaceutical, agrochemical, and materials science industries. Its versatility in chemical reactions makes it a valuable starting material for the creation of new molecules with desired properties.
Used in Research and Development:
Due to its unique chemical properties, 6-Aminocoumarin hydrochloride is also utilized in research and development settings. Scientists and researchers use it to study various chemical reactions and to develop new methodologies for the synthesis of complex organic molecules.

InChI:InChI=1/C9H7NO2.ClH/c10-7-2-3-8-6(5-7)1-4-9(11)12-8;/h1-5H,10H2;1H

Upstream product

• 14415-44-2 6-aminocoumarin 
• 91-64-5 coumarin 
• 2725-81-7 6-nitrocoumarin 

Downstream Products

• 1159275-30-5 (+/-)-6-([(6-bromo-2-methoxy-quinolin-3-yl)-phenylmethyl]-amino)-chromen-2-one 
• 130506-22-8 6-nitroso-1,2-benzopyrone 

Relevant articles and documents

Synthesis, structure, spectroscopic properties, electrochemistry, and DFT correlative studies of N-[(2-pyridyl)methyliden]-6-coumarin complexes of Cu(I) and Ag(I)

6-Aminocoumarin reacts with pyridine-2-carboxaldehyde and has synthesized N-[(2-pyridyl)methyliden]-6-coumarin (L). The ligand, L, reacts with [Cu(MeCN)4]ClO4/AgNO3 to synthesize Cu(I) and Ag(I) complexes of formulae, [Cu(L)2]ClO4 and [Ag(L) 2]NO3, respectively. While similar reaction in the presence of PPh3 has isolated [Cu(L)(PPh3) 2]ClO4 and [Ag(L)(PPh3)2]NO 3. All these compounds are characterized by FTIR, UV-Vis and 1H NMR spectroscopic data. In case of [Cu(L)(PPh3) 2]ClO4 and [Ag(L)(PPh3)2]NO 3, the structures have been confirmed by X-ray crystallography. The structure of the complexes are distorted tetrahedral in which L coordinates in a N,N′ bidentate fashion and other two coordination sites are occupied by PPh3. The ligand and the complexes are fluorescent and the fluorescence quantum yields of [Cu(L)(PPh3)2]ClO 4 and [Ag(L)(PPh3)2]NO3 are higher than [Cu(L)2]ClO4 and [Ag(L)2]NO3. Cu(I) complexes show Cu(II)/Cu(I) quasireversible redox couple while Ag(I) complexes exhibit deposition of Ag(0) on the electrode surface during cyclic voltammetric experiments. gaussian 03 computations of representative complexes have been used to determine the composition and energy of molecular levels. An attempt has been made to explain solution spectra and redox properties of the complexes.

6-amino-1,2-benzopyrones useful for treatment of viral diseases

Unsubstituted or substituted 6-amino-1,2-benzopyrones are potent, selective and non-toxic inhibitors and suppressants of viral infections in a mammalian host. The compounds are particularly useful for treatment of AIDS, herpetic episodes and cytomegaloviral infections. The method of treatment of viral diseases by 6-amino-1,2-benzopyrones is described.