1077-56-1 | N-Ethyl-O-Toluenesulfonamide

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$220.00	$154.00
250mg	95%	in stock	$389.00	$272.00
1g	95%	in stock	$786.00	$550.00

Description

• Catalog Number: AE08029
• Chemical Name: N-Ethyl-O-Toluenesulfonamide
• CAS Number: 1077-56-1
• Molecular Formula: C9H13NO2S
• Molecular Weight: 199.27001999999996
• MDL Number: MFCD00059226
• SMILES: CCNS(=O)(=O)c1ccccc1C

Computed Properties

• Complexity: 243
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.6

Upstream Synthesis Route

N-Ethyl-2-methylbenzenesulfonamide is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. This chemical plays a crucial role as a versatile building block in organic chemistry, particularly in the pharmaceutical and agrochemical industries.One of the key applications of N-Ethyl-2-methylbenzenesulfonamide is as a sulfonyl group transfer reagent. This compound can undergo various chemical reactions to transfer its sulfonyl group to other molecules, enabling the introduction of sulfonyl functionality into organic molecules. This reactivity makes N-Ethyl-2-methylbenzenesulfonamide a valuable tool for the synthesis of complex organic compounds.Furthermore, N-Ethyl-2-methylbenzenesulfonamide can also act as a protecting group in organic synthesis. By selectively masking reactive functional groups with the sulfonyl moiety, this compound allows chemists to control the course of a chemical reaction and protect specific parts of a molecule from unwanted reactions. This protection-deprotection strategy is commonly used in the efficient synthesis of complex molecules.Overall, the diverse applications of N-Ethyl-2-methylbenzenesulfonamide in chemical synthesis make it a valuable reagent for organic chemists working on the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.