CAS 3476-19-5

4-Bromo-N-propylbenzenesulfonamide

Description:

4-Bromo-N-propylbenzenesulfonamide is an organic compound characterized by its sulfonamide functional group, which is attached to a benzene ring that also features a bromine atom and a propyl substituent. This compound typically appears as a solid and is soluble in polar organic solvents. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and biological activity. The sulfonamide group is known for its antibacterial properties, making compounds like this of interest in medicinal chemistry. Additionally, the propyl group contributes to the hydrophobic character of the molecule, potentially affecting its interaction with biological systems. The compound's molecular structure allows for various applications, including in pharmaceuticals and as a building block in organic synthesis. Safety data indicates that, like many sulfonamides, it should be handled with care due to potential toxicity and allergic reactions. Overall, 4-Bromo-N-propylbenzenesulfonamide exemplifies the diverse functionalities that can be achieved through careful molecular design in organic chemistry.

Formula: C₉H₁₂BrNO₂S

InChI: InChI=1S/C9H12BrNO2S/c1-2-7-11-14(12,13)9-5-3-8(10)4-6-9/h3-6,11H,2,7H2,1H3

InChI key: InChIKey=CZRKEJQELXKHAQ-UHFFFAOYSA-N

SMILES: S(NCCC)(=O)(=O)C1=CC=C(Br)C=C1

Synonyms:

• Benzenesulfonamide, p-bromo-N-propyl-
• NSC 406257
• benzenesulfonamide, 4-bromo-N-propyl-
• 4-Bromo-N-propylbenzenesulfonamide

4-Bromo-N-propylbenzenesulfonamide

CAS: 3476-19-5

Formula: C₉H₁₂BrNO₂S

Molecular weight: 278.1661

Ref: IN-DA007CJW

4-Bromo-N-propylbenzenesulfonamide

CAS: 3476-19-5

Formula: C₉H₁₂BrNO₂S

Purity: 95.0%

Molecular weight: 278.16

Ref: 10-F217229

4-Bromo-N-propylbenzenesulfonamide

CAS: 3476-19-5

4-Bromo-N-propylbenzenesulfonamide is a tricyclic compound that has two skeletal carbons and three cyclic carbons. It is structurally similar to 4-bromobenzenesulfonyl chloride, but it lacks the sulfonyl group and instead has a sulfonamide group. The yields of this compound are high, with an average of 77% obtained from the reaction with 4-bromobenzoic acid. However, when there are substituents on the ring, such as in the case of 4-chloro-N-propylbenzenesulfonamide, the yield decreases significantly. This compound can be synthesized by reacting 4-bromoaniline with propylene oxide followed by reaction with bromosulfonic acid and sodium hydroxide.

Formula: C₉H₁₂BrNO₂S

Purity: Min. 95%

Molecular weight: 278.17 g/mol

Ref: 3D-DAA47619