CAS 7010-86-8

4-methoxy-N-methylbenzenesulfonamide

Description:

4-Methoxy-N-methylbenzenesulfonamide, with the CAS number 7010-86-8, is an organic compound characterized by its sulfonamide functional group, which is attached to a benzene ring that also features a methoxy group and a methylamine substituent. This compound typically appears as a white to off-white solid and is soluble in polar solvents due to the presence of the sulfonamide group, which enhances its polarity. The methoxy group contributes to its electronic properties, potentially influencing its reactivity and interactions with biological systems. As a sulfonamide, it may exhibit antibacterial properties, similar to other compounds in this class, although its specific biological activity would depend on its structure and substituents. The compound is of interest in medicinal chemistry and may serve as a lead compound for drug development or as a reagent in organic synthesis. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

Formula: C₈H₁₁NO₃S

InChI: InChI=1/C8H11NO3S/c1-9-13(10,11)8-5-3-7(12-2)4-6-8/h3-6,9H,1-2H3

InChI key: InChIKey=UIVZZDAOKBAWCS-UHFFFAOYSA-N

SMILES: S(NC)(=O)(=O)C1=CC=C(OC)C=C1

Synonyms:

• 4-Methoxy-N-methylbenzenesulfonamide
• N-Methyl-4-methoxybenzenesulfonamide
• Benzenesulfonamide, p-methoxy-N-methyl-
• Benzenesulfonamide, 4-methoxy-N-methyl-

4-Methoxy-N-methylbenzenesulfonamide

CAS: 7010-86-8

Formula: C₈H₁₁NO₃S

Purity: 95%

Color and Shape: Solid

Molecular weight: 201.2428

Ref: IN-DA00FD0D

4-Methoxy-N-methylbenzenesulphonamide

CAS: 7010-86-8

4-Methoxy-N-methylbenzenesulphonamide

Formula: C₈H₁₁NO₃S

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 201.24g/mol

Ref: 54-OR12490

4-METHOXY-N-METHYLBENZENESULFONAMIDE

CAS: 7010-86-8

Formula: C₈H₁₁NO₃S

Purity: 95.0%

Molecular weight: 201.24

Ref: 10-F539981

4-Methoxy-N-methylbenzenesulfonamide

CAS: 7010-86-8

4-Methoxy-N-methylbenzenesulfonamide is a synthetic organic chemical that is used as a catalyst in nitroso chemical reactions. The transition state for the reaction is kinetically controlled by the anions and the kinetic isotope effects. The substituent effects are important in determining how quickly the reaction proceeds, with electron withdrawing groups accelerating the rate of reaction. 4-Methoxy-N-methylbenzenesulfonamide can be used to transfer a proton from one molecule to another, which may lead to an imbalance of protons and/or electrons. This can result in a change in pH or redox potential, depending on whether it is transferring a proton from an acid or base.

Formula: C₈H₁₁NO₃S

Purity: Min. 95%

Molecular weight: 201.24 g/mol

Ref: 3D-HAA01086