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3-Hydroxymethyl-1H-quinolin-2-one, a quinolinone derivative with the molecular formula C10H9NO2, features a hydroxymethyl group attached to the quinoline ring. This chemical compound has garnered interest in medicinal chemistry due to its diverse potential applications, including antibacterial, antifungal, chelating, and fluorescent dye properties, as well as its utility in organic synthesis and coordination chemistry.

90097-45-3

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90097-45-3 Usage

Uses

Used in Pharmaceutical Industry:
3-Hydroxymethyl-1H-quinolin-2-one is used as an active pharmaceutical ingredient for its antibacterial and antifungal properties, offering potential treatments for various infections caused by resistant strains of bacteria and fungi.
Used in Chemical Research:
3-HYDROXYMETHYL-1H-QUINOLIN-2-ONE serves as a chelating agent, enabling the binding of metal ions, which is crucial in various chemical processes and reactions, including the synthesis of metal-organic frameworks and catalysis.
Used in Organic Synthesis:
3-Hydroxymethyl-1H-quinolin-2-one is utilized as a building block in organic synthesis, contributing to the creation of complex organic molecules and pharmaceuticals.
Used in Materials Science:
As a fluorescent dye, 3-hydroxymethyl-1H-quinolin-2-one has potential applications in the development of sensors, imaging agents, and other optoelectronic devices due to its light-emitting properties.
Used in Coordination Chemistry:
3-HYDROXYMETHYL-1H-QUINOLIN-2-ONE functions as a ligand in coordination chemistry, forming complexes with metal ions to create new materials with unique properties, such as catalysts, pharmaceuticals, and materials with specific electronic or magnetic characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 90097-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90097-45:
(7*9)+(6*0)+(5*0)+(4*9)+(3*7)+(2*4)+(1*5)=133
133 % 10 = 3
So 90097-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c12-6-8-5-7-3-1-2-4-9(7)11-10(8)13/h1-5,12H,6H2,(H,11,13)

90097-45-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxymethyl)-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names hydroxymethylquinolinone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90097-45-3 SDS

90097-45-3Relevant academic research and scientific papers

Design of new quinolin-2-one-pyrimidine hybrids as sphingosine kinases inhibitors

Abonia, Rodrigo,Andújar, Sebastián,Cobo, Justo,Enriz, Ricardo D.,Gutiérrez, Lucas,Insuasty, Daniel,Lima, Santiago,Marchal, Antonio,Nogueras, Manuel,Spiegel, Sarah,Vettorazzi, Marcela

, (2019/12/09)

Sphingosine-1-phosphate is now emerging as an important player in cancer, inflammation, autoimmune, neurological and cardiovascular disorders. Abundance evidence in animal and humans cancer models has shown that SphK1 is linked to cancer. Thus, there is a

Applications of Baylis-Hillman chemistry: One-pot convenient synthesis of functionalized (1H)-quinol-2-ones and quinolines

Basavaiah, Deevi,Reddy, Ravi Mallikarjuna,Kumaragurubaran, Nagaswamy,Sharada, Duddu S

, p. 3693 - 3697 (2007/10/03)

A simple synthesis of functionalized (1H)-quinol-2-ones and quinolines from the Baylis-Hillman adducts, i.e. alkyl 3-hydroxy-2-methylene-3-arylpropanoates and β-hydroxy-α-methylene-β-arylalkanones, respectively, has been described.

Carbostyril derivatives

-

, (2008/06/13)

Disclosed are carbostyril derivatives and their salts of the formulas STR1 The compounds have anti-peptic ulcer effects, and are useful as a treating agent for curing peptic ulcers in the digestive system, such as ulcers in the stomach and in the duodenum. The compounds particularly have prophylaxis and curing effects for treating chronic ulcers, for example experimental acetic acid-induced ulcers and cautery ulcers, with both low toxicity and few side-effects. Also disclosed are processes for preparing the compounds and for preparing pharmaceutical compositions containing them.

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