4254-29-9 | 2-Indanol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
5g	98%	in stock	$17.00	$12.00
25g	98%	in stock	$55.00	$39.00
100g	98%	in stock	$143.00	$100.00
500g	98%	in stock	$572.00	$400.00

Description

• Catalog Number: AI50276
• Chemical Name: 2-Indanol
• CAS Number: 4254-29-9
• Molecular Formula: C9H10O
• Molecular Weight: 134.1751
• MDL Number: MFCD00003800
• SMILES: OC1Cc2c(C1)cccc2
• NSC Number: 17485

Computed Properties

• Complexity: 108
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

2,3-Dihydro-1H-inden-2-ol, also known as indeneol, serves as a versatile building block in chemical synthesis due to its unique structural properties and reactivity. This compound acts as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fragrances. Its cyclohexenone moiety makes it a valuable starting material for the synthesis of complex organic molecules. Additionally, the presence of a hydroxyl group in its structure allows for further functionalization, enabling the introduction of various substituents to tailor the molecule for specific applications. In organic chemistry, 2,3-Dihydro-1H-inden-2-ol is utilized in the preparation of heterocyclic compounds, natural product synthesis, and as a precursor for the construction of chiral molecules. Its versatile nature and ability to undergo diverse chemical transformations make it a valuable tool for organic chemists in the design and development of novel compounds.

Literature

• Spectroscopic and computational studies of the intramolecular hydrogen bonding of 2-indanol.

  The journal of physical chemistry. A 20061109

• Resonantly enhanced multiphoton ionization and zero kinetic energy photoelectron spectroscopy of 2-indanol conformers.

  The Journal of chemical physics 20060528

• Development of highly stereoselective asymmetric 6pi-azaelectrocyclization of conformationally flexible linear 1-azatrienes. from determination of multifunctional chiral amines, 7-alkyl cis-1-amino-2-indanols, to application as a new synthetic strategy: formal synthesis of 20-epiuleine.

  The Journal of organic chemistry 20040903