CAS 35303-76-5

4-(2-Aminoethyl)benzenesulfonamide

Description:

4-(2-Aminoethyl)benzenesulfonamide, also known as a sulfonamide compound, is characterized by its sulfonamide functional group (-SO2NH2) attached to a benzene ring, which is further substituted with an aminoethyl group. This structure imparts both hydrophilic and hydrophobic properties, making it soluble in polar solvents while retaining some lipophilicity due to the aromatic ring. The compound typically exhibits a white to off-white crystalline appearance and has a moderate melting point. It is known for its potential biological activity, particularly in medicinal chemistry, where sulfonamides have been utilized as antibacterial agents. The aminoethyl side chain can participate in hydrogen bonding, enhancing its interaction with biological targets. Additionally, the presence of the sulfonamide group contributes to its acidity, allowing it to act as a weak acid in solution. Overall, 4-(2-Aminoethyl)benzenesulfonamide is a versatile compound with applications in pharmaceuticals and biochemistry, particularly in the development of drugs targeting bacterial infections.

Formula: C₈H₁₂N₂O₂S

InChI: InChI=1S/C8H12N2O2S/c9-6-5-7-1-3-8(4-2-7)13(10,11)12/h1-4H,5-6,9H2,(H2,10,11,12)

InChI key: InChIKey=FXNSVEQMUYPYJS-UHFFFAOYSA-N

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

Synonyms:

• 2-(4-Sulfamoylphenyl)ethylamine
• 2-[4-(Aminosulfonyl)phenyl]ethylamine
• 4-(2-Aminoethyl)Benzene Sulfonmide
• 4-(2-Aminoethyl)Benzene Sulphonamide
• 4-(2-Aminoethyl)Benzenesulfonamide (Intermediate Of Glibenclamide,Glipizide,Gliquidone)
• 4-(2-Aminoethyl)benzensulfonamide
• 4-(2-Aminoethyl)benzesulfonamide
• 4-(2-Ethylamino) Benzene Sulfonamide
• 4-(Aminosulfonyl)phenethylamine
• 4-Aminoethyl benzenesulfonamide
• 4-Aminoethylbenzenesulfonamide
• 4-Sulfamoylphenethylamine
• Benzenesulfonamide, 4-(2-aminoethyl)-
• Benzenesulfonamide, p-(2-aminoethyl)-
• Labotest-Bb Lt00080735
• Otava-Bb Bb7020410047
• P-(2-Aminoethyl)Benzenesulfonamide
• Timtec-Bb Sbb003544
• p-(β-Aminoethyl)benzenesulfonamide
• p-Aminoethyl-benzenesulfonamide
• 4-(2-Aminoethyl)benzenesulfonamide

4-(2-Aminoethyl)benzenesulfonamide

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Orange to Green powder to crystal

Molecular weight: 200.26

Ref: 3B-A1363

4-(2-Aminoethyl)benzenesulfonamide

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 200.2581

Ref: IN-DA0037CO

Glipizide Impurity 11

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Color and Shape: White To Off-White Solid

Molecular weight: 200.26

Ref: 4Z-G-1122

4-(2-Aminoethyl)benzenesulfonamide

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Molecular weight: 200.26

Ref: 7W-GK1789

4-(2-Aminoethyl)benzenesulphonamide

CAS: 35303-76-5

4-(2-Aminoethyl)benzenesulphonamide

Formula: C₈H₁₂N₂O₂S

Purity: ≥95%

Color and Shape: white crystalline powder

Molecular weight: 200.26g/mol

Ref: 54-OR9989

4-(2-Aminoethyl)benzenesulfonamide

CAS: 35303-76-5

Color and Shape: Neat

Ref: 86-MM0942.10

4-(2-Aminoethyl)benzenesulfonamide

Controlled Product

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Color and Shape: Neat

Molecular weight: 200.26

Ref: TR-A608790

4-(2-Aminoethyl)benzenesulfonamide

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Purity: 95.0%

Color and Shape: Solid, White - Slightly pale reddish yellow powder

Molecular weight: 200.26

Ref: 10-F210409

4-(2-Aminoethyl)benzene sulfonamide

CAS: 35303-76-5

4-(2-Aminoethyl)benzene sulfonamide is a small-molecule drug that inhibits the activity of proteases, including serine and cysteine proteases. It has been shown to inhibit the growth of human renal cell cancer cells, as well as subcutaneous tumors in mice. 4-(2-Aminoethyl)benzene sulfonamide also inhibits the proliferation of Hl-60 cells and shows antitumor activity in a mouse model system. This drug is an inhibitor of prostaglandin endoperoxide synthase (PGHS), which is involved in tumorigenesis by causing inflammation and oxidative stress. 4-(2-Aminoethyl)benzene sulfonamide has been shown to be effective for treating colorectal adenocarcinoma, with no significant side effects on other organs.

Formula: C₈H₁₂N₂O₂S

Purity: Min. 95%

Molecular weight: 200.26 g/mol

Ref: 3D-FA10909

Glipizide Impurity 11

CAS: 35303-76-5

Formula: C₈H₁₂N₂O₂S

Molecular weight: 200.26

Ref: ST-EA-CP-G11033