621-87-4 | 1-Phenoxypropan-2-one

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$26.00	$18.00
5g	97%	in stock	$28.00	$19.00
10g	97%	in stock	$45.00	$31.00
25g	97%	in stock	$86.00	$60.00

Description

• Catalog Number: AB78232
• Chemical Name: 1-Phenoxypropan-2-one
• CAS Number: 621-87-4
• Molecular Formula: C9H10O2
• Molecular Weight: 150.1745
• MDL Number: MFCD00008767
• SMILES: CC(=O)COc1ccccc1
• NSC Number: 1876

Computed Properties

• Complexity: 126
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 1

Upstream Synthesis Route

1-Phenoxypropan-2-one, also known as phenyl propionyl ether, is a versatile compound used in various chemical synthesis processes. This organic compound serves as a valuable building block for the synthesis of a wide range of chemicals and pharmaceuticals. Due to its unique chemical structure, 1-Phenoxypropan-2-one is commonly utilized as a key intermediate in the production of fragrances, flavors, and pharmaceutical ingredients.In chemical synthesis, 1-Phenoxypropan-2-one acts as a crucial precursor for the preparation of diverse compounds through functional group transformations. Its reactivity allows for the introduction of different functional groups, facilitating the creation of complex molecules in a controlled manner. The presence of the phenoxy group in the molecule provides opportunities for further derivatization through various chemical reactions, making it a versatile starting material in organic synthesis.Moreover, 1-Phenoxypropan-2-one's compatibility with a wide range of reagents and reaction conditions makes it a preferred choice for chemists seeking to introduce the propionyl ether moiety into target molecules. This compound's role in chemical synthesis extends to the creation of pharmaceutical intermediates, agrochemicals, and fine chemicals, highlighting its importance in the field of organic chemistry.Overall, the application of 1-Phenoxypropan-2-one in chemical synthesis showcases its significance as a valuable tool for generating intricate chemical structures and advancing innovation in the production of diverse compounds.

Literature

• Chemical composition and insecticidal activity of the essential oil of Amethystea caerulea L.

  Natural product research 20120101

• Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling.

  The Journal of organic chemistry 20100521

• Calixpyrrole chemistry: a study of a new ditopic receptor highlighting some fundamental concepts in assessing thermodynamic selectivity.

  Physical chemistry chemical physics : PCCP 20100121