10342-83-3 | 4'-Bromopropiophenone

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$15.00	$10.00
5g	95%	in stock	$16.00	$11.00
25g	95%	in stock	$19.00	$13.00
500g	95%	in stock	$231.00	$162.00

Description

• Catalog Number: AD48031
• Chemical Name: 4'-Bromopropiophenone
• CAS Number: 10342-83-3
• Molecular Formula: C9H9BrO
• Molecular Weight: 213.0712
• MDL Number: MFCD00000106
• SMILES: CCC(=O)c1ccc(cc1)Br
• NSC Number: 83574

Computed Properties

• Complexity: 137
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 3.1

Upstream Synthesis Route

1-(4-Bromophenyl)propan-1-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its primary application lies in organic chemistry, where it serves as a key intermediate in the production of various compounds.In chemical synthesis, $name$ plays a crucial role as a building block for creating more complex molecules. Its unique structure containing a bromine substituent on a phenyl ring and a propanone functional group enables it to participate in a wide range of reactions, such as nucleophilic substitution, Friedel-Crafts acylation, and Grignard reactions.$name$ is commonly used in the pharmaceutical industry for the synthesis of pharmaceutical drugs, as well as in the development of agrochemicals and fine chemicals. Its reactivity and compatibility with a variety of functional groups make it a valuable tool for synthetic chemists seeking to design and produce new compounds with specific properties and applications.Furthermore, $name$ finds applications in academic research, where it is employed in the study of reaction mechanisms, structure-activity relationships, and the development of new synthetic methodologies. Its presence in the chemical toolbox of researchers and industrial chemists highlights its importance as a versatile and foundational compound in modern organic synthesis.

Literature

• Chemoselective synthesis of ketones and ketimines by addition of organometallic reagents to secondary amides.

  Nature chemistry 20120221