25177-85-9 | 2-Indanecarboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$6.00
5g	98%	in stock	$19.00	$14.00
10g	98%	in stock	$37.00	$26.00
25g	98%	in stock	$91.00	$64.00
100g	98%	in stock	$363.00	$255.00

Description

• Catalog Number: AB27799
• Chemical Name: 2-Indanecarboxylic acid
• CAS Number: 25177-85-9
• Molecular Formula: C10H10O2
• Molecular Weight: 162.1852
• MDL Number: MFCD00085095
• SMILES: OC(=O)C1Cc2c(C1)cccc2

Computed Properties

• Complexity: 174
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.7

Upstream Synthesis Route

2,3-Dihydro-1H-indene-2-carboxylic acid is a versatile compound commonly utilized in chemical synthesis for its unique properties. This compound serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. Its cyclic structure and carboxylic acid functionality make it a key intermediate in the preparation of a wide range of complex molecules.In organic synthesis, 2,3-Dihydro-1H-indene-2-carboxylic acid can be employed to introduce the indene motif into target molecules, imparting specific chemical and biological properties. The carboxylic acid group enables further functionalization through various chemical reactions, allowing for the modification of the compound to meet specific requirements in the synthesis process.Furthermore, this compound can participate in diverse transformation reactions such as esterification, amidation, and condensation reactions, expanding its utility in building molecular complexity. Its structural flexibility and reactivity provide synthetic chemists with a valuable tool for designing and accessing structurally diverse compounds for research and development purposes.Overall, 2,3-Dihydro-1H-indene-2-carboxylic acid plays a crucial role in modern chemical synthesis strategies, offering a platform for the construction of intricate molecules with potential applications in various industries.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101