2987-49-7 | 2-(Methylsulfonyl)aniline

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$33.00	$24.00
5g	98%	in stock	$99.00	$70.00
10g	98%	in stock	$163.00	$115.00
100g	98%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AF37757
• Chemical Name: 2-(Methylsulfonyl)aniline
• CAS Number: 2987-49-7
• Molecular Formula: C7H9NO2S
• Molecular Weight: 171.2169
• MDL Number: MFCD08444390
• SMILES: Nc1ccccc1S(=O)(=O)C
• NSC Number: 55747

Computed Properties

• Complexity: 217
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.9

Upstream Synthesis Route

2-(Methanesulfonyl)aniline is a versatile compound that finds wide application in chemical synthesis due to its unique properties. It serves as a crucial building block in organic chemistry, particularly in the preparation of various pharmaceuticals, agrochemicals, and functional materials.One of the key applications of 2-(Methanesulfonyl)aniline is its use as a sulfonylating agent in organic reactions. The methanesulfonyl group (-SO2CH3) is a powerful and versatile functional group that can be easily manipulated to introduce diverse functionalities into molecules. This compound is frequently employed in sulfonation reactions to introduce the methanesulfonyl moiety into organic substrates, thereby enabling further modifications and functionalizations through subsequent transformations.Moreover, 2-(Methanesulfonyl)aniline is utilized as a protecting group in organic synthesis to block specific functional groups temporarily, safeguarding them from undesired reactions or transformations during the course of a multistep synthesis. Once the desired modifications are complete, the methanesulfonyl group can be selectively removed under mild conditions to reveal the reactive functional group for further elaboration.In summary, 2-(Methanesulfonyl)aniline plays a crucial role in chemical synthesis as a versatile compound for sulfonylation reactions and as a protecting group, enabling the efficient and selective modification of organic molecules in the synthesis of various valuable compounds.