3466-32-8 | 4-Bromophenyl methyl sulfone

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$6.00
5g	98%	in stock	$10.00	$7.00
10g	98%	in stock	$16.00	$12.00
25g	98%	in stock	$29.00	$21.00

Description

• Catalog Number: AI48478
• Chemical Name: 4-Bromophenyl methyl sulfone
• CAS Number: 3466-32-8
• Molecular Formula: C7H7BrO2S
• Molecular Weight: 235.0983
• MDL Number: MFCD00025065
• SMILES: Brc1ccc(cc1)S(=O)(=O)C
• NSC Number: 174742

Computed Properties

• Complexity: 209
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

1-Bromo-4-(methylsulfonyl)benzene is a versatile chemical compound that finds its application in various chemical synthesis processes. This compound is commonly used as a building block in organic synthesis due to its unique structure and reactivity. The presence of a bromine atom on the benzene ring makes 1-Bromo-4-(methylsulfonyl)benzene an excellent electrophile, allowing it to participate in various substitution reactions. Additionally, the methylsulfonyl group provides an anchor for introducing functional groups, enabling further derivatization of the molecule.In organic synthesis, 1-Bromo-4-(methylsulfonyl)benzene can be utilized in the construction of complex molecules such as pharmaceuticals, agrochemicals, and materials. It can serve as a precursor for the synthesis of biologically active compounds or as a linker in the formation of molecular scaffolds.Moreover, the unique combination of bromine and methylsulfonyl functionalities in 1-Bromo-4-(methylsulfonyl)benzene offers chemists a strategic tool for designing novel molecules with tailored properties. Its compatibility with various reaction conditions makes it a valuable reagent for synthetic chemists aiming to access diverse chemical space and develop innovative synthetic routes.

Literature

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

  Bioorganic & medicinal chemistry letters 20101101