615-13-4 | 2-Indanone

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$13.00	$9.00
10g	98%	in stock	$21.00	$15.00
25g	98%	in stock	$26.00	$18.00
100g	98%	in stock	$50.00	$35.00
500g	98%	in stock	$192.00	$135.00

Description

• Catalog Number: AB62382
• Chemical Name: 2-Indanone
• CAS Number: 615-13-4
• Molecular Formula: C9H8O
• Molecular Weight: 132.1592
• MDL Number: MFCD00003792
• SMILES: O=C1Cc2c(C1)cccc2

Computed Properties

• Complexity: 135
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 1.3

Upstream Synthesis Route

2-Indanone, also known as 2-hydroxyindane or isatin, is a versatile organic compound with various applications in chemical synthesis. In organic chemistry, 2-indanone serves as a key starting material for the synthesis of a wide range of important compounds due to its unique structural properties.One of the primary applications of 2-indanone is as a precursor in the synthesis of pharmaceuticals and agrochemicals. Its ability to undergo various chemical transformations, such as nucleophilic addition, oxidation, and reduction reactions, makes it a valuable building block in the pharmaceutical industry. By functionalizing the carbonyl group or modifying the ring structure of 2-indanone, chemists can create diverse drug candidates with potential therapeutic benefits.Additionally, 2-indanone plays a crucial role in the synthesis of natural products and fine chemicals. Its aromatic ring system and carbonyl functionality provide opportunities for chemists to manipulate its structure and stereochemistry, enabling the creation of complex molecules with specific biological activities. From synthesizing natural alkaloids to designing novel materials, the versatility of 2-indanone in chemical synthesis makes it a valuable tool for researchers across various fields of chemistry.

Literature

• Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics.

  The Journal of organic chemistry 20110701

• Calculation of the vibrationally resolved, circularly polarized luminescence of d-camphorquinone and (S,S)-trans-beta-hydrindanone.

  Chemphyschem : a European journal of chemical physics and physical chemistry 20100802

• Diastereoisomers of 2-benzyl-2, 3-dihydro-2-(1H-inden-2-yl)-1H-inden-1-ol: potential anti-inflammatory agents.

  Bioorganic & medicinal chemistry letters 20091015

• Bacterial degradation of aromatic compounds.

  International journal of environmental research and public health 20090101

• Calorimetric and computational study of indanones.

  The journal of physical chemistry. A 20071101

• Experimental study on the thermal oxidation of 2-chlorophenol in air over the temperature range 450-900 degrees C.

  Chemosphere 20060301

• Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3.

  FEMS microbiology letters 20050815

• Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.

  Journal of medicinal chemistry 20050602

• Lipoprotein mutation accelerates substrate permeability-limited toluene dioxygenase-catalyzed reaction.

  Biotechnology progress 20050101

• Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism.

  The Journal of organic chemistry 20030404

• Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes.

  Organic letters 20020725

• New metabolites in the degradation of fluorene by Arthrobacter sp. strain F101.

  Applied and environmental microbiology 19970301