3470-45-9 | 1-Indanone-5-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$47.00	$33.00
250mg	98%	in stock	$66.00	$47.00
1g	98%	in stock	$238.00	$167.00
5g	98%	in stock	$661.00	$463.00
10g	98%	in stock	$1,123.00	$787.00

Description

• Catalog Number: AF57299
• Chemical Name: 1-Indanone-5-carboxylic acid
• CAS Number: 3470-45-9
• Molecular Formula: C10H8O3
• Molecular Weight: 176.1687
• MDL Number: MFCD03411486
• SMILES: OC(=O)c1ccc2c(c1)CCC2=O

Computed Properties

• Complexity: 247
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.2

Upstream Synthesis Route

1-Indanone-5-carboxylic acid, also known as indanone-5-carboxylic acid, is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.One of the significant applications of 1-Indanone-5-carboxylic acid is its role as a precursor in the synthesis of heterocyclic compounds such as indole derivatives. By undergoing various transformations, such as cyclization reactions and functional group modifications, this compound can be used to generate a diverse range of biologically active molecules. These derivatives exhibit a wide spectrum of pharmacological activities, making them valuable intermediates in drug discovery and development.In addition to its importance in pharmaceutical chemistry, 1-Indanone-5-carboxylic acid is also utilized in the preparation of specialty chemicals and materials. Its functional groups can be selectively modified to introduce specific properties or functionalities into the final products. This versatility makes it a valuable starting material for producing a variety of compounds used in industrial applications.Overall, the strategic placement of the carboxylic acid group in the indanone structure of this compound enables precise control over its reactivity, allowing for efficient and selective transformations in chemical synthesis. Its broad utility in the creation of complex molecules highlights its significance as a key component in organic chemistry research and development.