CAS 144-80-9

N-Sulfanilylacetamide

Description:

N-Sulfanilylacetamide, with the CAS number 144-80-9, is a chemical compound that belongs to the class of sulfanilamide derivatives. It is characterized by the presence of a sulfonamide functional group, which is known for its antibacterial properties. This compound typically appears as a white to off-white crystalline solid and is soluble in water and organic solvents, making it versatile for various applications. N-Sulfanilylacetamide is primarily used in pharmaceutical formulations and research, particularly in the development of antimicrobial agents. Its structure includes an acetamide group, which contributes to its biological activity. The compound is known to exhibit moderate toxicity, and safety precautions should be taken when handling it. Additionally, it may undergo hydrolysis and other chemical reactions under certain conditions, which can affect its stability and efficacy. Overall, N-Sulfanilylacetamide is an important compound in medicinal chemistry, particularly in the context of developing treatments for bacterial infections.

Formula: C₈H₁₀N₂O₃S

InChI: InChI=1/C6H7NO3/c1-4(8)7-5(9)2-3-6(7)10/h2-3H2,1H3

InChI key: InChIKey=SKIVFJLNDNKQPD-UHFFFAOYSA-N

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

Synonyms:

• 1-Acetylpyrrolidine-2,5-Dione
• 4-(Acetylaminosulfonyl)aniline
• A-500
• Acetamide, N-[(4-aminophenyl)sulfonyl]-
• Acetamide, N-sulfanilyl-
• Acetocid
• Acetosulfamin
• Acetosulfamine
• Albamine
• Albucid
• Alesten
• Formosulfacetamide
• N'-Acetylsulfanilamide
• N-(4-Aminobenzenesulfonyl)acetamide
• N-(4-Aminobenzenesulphonyl)acetamide
• N-(4-Aminophenylsulphonyl)acetamide
• N-(p-Aminophenylsulfonyl)acetamide
• N-[(4-Aminophenyl)sulfonyl]acetamide
• N-sulphanilylacetamide
• N1-Acetylsulfanilamide
• N¹-Acetylsulfanilamide
• Nsc 63871
• Ocusol
• Region
• Steramide
• Sulamyd
• Sulfacet
• Sulfacetamid
• Sulfacetamida
• Sulfacetamide
• Sulfacetamide Free Base
• Sulfacetimide
• Sulfacyl
• Sulphacetamide
• Sulphasil
• Urosulfon
• p-Aminobenzenesulfonacetamide
• N-[P-AMINOBENZENESULFONYL]ACETAMIDE
• AKOS BBB/023
• N-SULFANILYACETAMIDE
• N-(4-AMINOPHENYLSULFONYL)ACETAMIDE
• sultrin
• LABOTEST-BB LT00053160
• N-ACETYL-4-AMINO-BENZENESULFONAMIDE
• sulfanilacetamide
• N'-ACETYLSUFANILAMIDE

Sulfacetamide in Methanol

CAS: 144-80-9

Methanol

Ref: BE-BePure-25655XM-100

Sulfacetamide

CAS: 144-80-9

N-((4-Aminophenyl)sulfonyl)acetamide

Formula: C₈H₁₀N₂O₃S

Purity: 98%

Molecular weight: 214.24

Ref: IN-DG152135

N-((4-Aminophenyl)sulfonyl)acetamide

CAS: 144-80-9

Formula: C₈H₁₀N₂O₃S

Purity: 98%

Color and Shape: No data available.

Molecular weight: 214.24

Ref: 10-F226015

Sulfacetamide (DISCONTINUED)

CAS: 144-80-9

Sulfonamides used as drugs

Formula: C₈H₁₀N₂O₃S

Color and Shape: White Crystalline Powder

Molecular weight: 214.04121

Ref: 45-1623808

Sulfacetamide

CAS: 144-80-9

Sulfacetamide is an antimicrobial agent that is used in the treatment of infectious diseases. The optimum concentration for sulfacetamide is between 0.2 and 1 mg/L, and it has inhibitory properties against Gram-positive bacteria such as S. aureus and S. pyogenes. Sulfacetamide has been shown to be effective in wastewater treatment by inhibiting the growth of bacteria that are resistant to other antibiotics, such as tetracycline and erythromycin. It also shows inhibitory activity against Gram-negative bacteria such as E. coli, Klebsiella pneumoniae, and Salmonella enterica serovar Typhimurium. The chemical structure of sulfacetamide consists of a sulfonamide group (S=O) with a carbonyl group (-C=O) attached to the sulfur atom (S). This structure allows it to act as an inhibitor of bacterial enzymes responsible for synthesizing proteins from amino acids or

Formula: C₈H₁₀N₂O₃S

Purity: Min. 95%

Molecular weight: 214.24 g/mol

Ref: 3D-FS61457