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3,4-Dihydro-2-(1H)-quinolinone, 98%, Thermo Scientific Chemicals
Catalog number: H36638.03
1 g, Each
Thermo Scientific Chemicals
3,4-Dihydro-2-(1H)-quinolinone, 98%, Thermo Scientific Chemicals
Catalog number: H36638.03
1 g, Each
Quantity
Catalog number: H36638.03
also known as H36638-03
Price (USD)
49.20
Each
Quantity
-
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Chemical Identifiers
CAS
553-03-7
IUPAC Name
1,2,3,4-tetrahydroquinolin-2-one
Molecular Formula
C9H9NO
InChI Key
TZOYXRMEFDYWDQ-UHFFFAOYSA-N
SMILES
O=C1CCC2=CC=CC=C2N1
Specifications
Specification SheetForm
Powder
Assay (GC)
≥97.5%
Melting Point (clear melt)
163-171°C
Appearance (Color)
White to cream to pale brown
Description
3,4-Dihydro-2-(1H)-quinolinone may be employed as medium supplement in the culture medium of Pseudomonas ayucida during enrichment culture experiments. It is used to prepare potent bicyclic peptide deformylase inhibitors with antibacterial effects. It is also used to synthesize substituted iminopiperidines as inhibitors of human nitric oxide synthase isoforms.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3,4-Dihydro-2-(1H)-quinolinone may be employed as medium supplement in the culture medium of Pseudomonas ayucida during enrichment culture experiments. It is used to prepare potent bicyclic peptide deformylase inhibitors with antibacterial effects. It is also used to synthesize substituted iminopiperidines as inhibitors of human nitric oxide synthase isoforms.
Solubility
Slightly soluble in water.
Notes
Light sensitive. Incompatible with oxidizing agents.
3,4-Dihydro-2-(1H)-quinolinone may be employed as medium supplement in the culture medium of Pseudomonas ayucida during enrichment culture experiments. It is used to prepare potent bicyclic peptide deformylase inhibitors with antibacterial effects. It is also used to synthesize substituted iminopiperidines as inhibitors of human nitric oxide synthase isoforms.
Solubility
Slightly soluble in water.
Notes
Light sensitive. Incompatible with oxidizing agents.
RUO – Research Use Only
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