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Home  > 2-Hydroxy-8-methylquinoline-3-carbaldehyde

AA05449

101382-54-1 | 2-Hydroxy-8-methylquinoline-3-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $130.00 $91.00 -   +
250mg 95% in stock $216.00 $151.00 -   +
1g 95% in stock $235.00 $164.00 -   +
5g 95% in stock $895.00 $626.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA05449
Chemical Name: 2-Hydroxy-8-methylquinoline-3-carbaldehyde
CAS Number: 101382-54-1
Molecular Formula: C11H9NO2
Molecular Weight: 187.1947
MDL Number: MFCD02227049
SMILES: O=Cc1cc2cccc(c2[nH]c1=O)C

 

Computed Properties
Complexity: 296  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.4  

 

 

Upstream Synthesis Route
  • 2-Hydroxy-8-methylquinoline-3-carbaldehyde, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, 2-Hydroxy-8-methylquinoline-3-carbaldehyde serves as a valuable building block in the synthesis of complex molecules.One of the notable applications of 2-Hydroxy-8-methylquinoline-3-carbaldehyde is its role as a precursor in the synthesis of heterocyclic compounds. By undergoing various functional group transformations, this compound can be used to construct a diverse range of heterocycles with specific properties and applications. Additionally, 2-Hydroxy-8-methylquinoline-3-carbaldehyde is employed in the preparation of chiral ligands, which are indispensable in asymmetric synthesis for the production of enantiopure compounds.Furthermore, 2-Hydroxy-8-methylquinoline-3-carbaldehyde is utilized in the development of fluorescent probes and dyes. Its ability to undergo selective reactions and exhibit fluorescence properties makes it a promising candidate for generating molecular probes for biological imaging and detection applications. The versatility of this compound in chemical synthesis highlights its significance in advancing various research fields and industrial processes.
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