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AE11710

1092351-51-3 | 1-Methyl-1H-indazole-6-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $20.00 $14.00 -   +
1g 98% in stock $54.00 $38.00 -   +
5g 98% in stock $233.00 $164.00 -   +
10g 98% in stock $466.00 $327.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE11710
Chemical Name: 1-Methyl-1H-indazole-6-carbaldehyde
CAS Number: 1092351-51-3
Molecular Formula: C9H8N2O
Molecular Weight: 160.1726
MDL Number: MFCD11109366
SMILES: Cn1ncc2c1cc(C=O)cc2

 

Computed Properties
Complexity: 183  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 1.6  

 

 

Upstream Synthesis Route
  • 1-Methyl-1H-indazole-6-carbaldehyde, a versatile building block in organic chemistry, plays a crucial role in chemical synthesis as a key intermediate. This compound is commonly utilized for the efficient preparation of various heterocyclic compounds, pharmaceuticals, and agrochemicals. Its unique structural features make it an ideal candidate for the construction of diverse molecular scaffolds through a range of synthetic transformations.In organic synthesis, 1-Methyl-1H-indazole-6-carbaldehyde serves as a valuable starting material for the synthesis of biologically active molecules and natural products. Its reactivity allows for the introduction of functional groups at specific positions on the indazole ring, enabling the design and synthesis of novel compounds with potential pharmacological properties. Additionally, its use in transition metal-catalyzed reactions facilitates the construction of complex molecular architectures with high efficiency and selectivity.Furthermore, the presence of the aldehyde group in 1-Methyl-1H-indazole-6-carbaldehyde offers opportunities for further derivatization through various chemical transformations such as reduction, oxidation, and nucleophilic addition reactions. This versatility in functional group manipulation enhances the compound's synthetic utility and broadens its applications in medicinal chemistry, materials science, and other interdisciplinary fields.
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