1186509-61-4 | 1-Benzylindazole-3-carbaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$121.00	$85.00
1g	98%	in stock	$289.00	$203.00
5g	98%	in stock	$921.00	$645.00
25g	98%	in stock	$3,089.00	$2,162.00

Description

• Catalog Number: AI11988
• Chemical Name: 1-Benzylindazole-3-carbaldehyde
• CAS Number: 1186509-61-4
• Molecular Formula: C15H12N2O
• Molecular Weight: 236.2686
• MDL Number: MFCD22571299
• SMILES: O=Cc1nn(c2c1cccc2)Cc1ccccc1

Computed Properties

• Complexity: 288
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 3

Upstream Synthesis Route

1-Benzylindazole-3-carbaldehyde is a versatile chemical compound widely used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This aromatic aldehyde plays a crucial role in organic chemistry due to its unique structure and reactivity.In chemical synthesis, 1-Benzylindazole-3-carbaldehyde serves as a valuable intermediate in the preparation of diverse organic compounds. Its aldehyde group is a common site for further functionalization through various reactions, such as Grignard reactions, Wittig reactions, and nucleophilic additions. This allows for the modification of its structure to introduce specific properties or functionalities required for the desired end product.Additionally, the indazole ring in 1-Benzylindazole-3-carbaldehyde provides opportunities for diversification and elaboration, enabling the synthesis of complex molecules with potential biological activities or industrial applications. Its presence in the molecular framework imparts unique characteristics to the final products, making it a valuable scaffold in drug discovery and development.Overall, the application of 1-Benzylindazole-3-carbaldehyde in chemical synthesis offers chemists a powerful tool for constructing novel compounds, exploring new reaction pathways, and designing functional materials with tailored properties. Its versatility and utility make it a valuable reagent in modern organic synthesis strategies, contributing to advancements in medicinal chemistry, materials science, and other fields.