CAS 6633-76-7

2-(4-aminophenyl)acetamide

Description:

2-(4-Aminophenyl)acetamide, also known as para-aminophenylacetamide, is an organic compound characterized by its amide functional group and an amino group attached to a phenyl ring. It typically appears as a white to off-white crystalline solid. The compound is soluble in water and organic solvents, reflecting its polar nature due to the presence of both the amine and amide groups. It has a moderate melting point and is stable under standard conditions. This substance is often studied for its potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of various drugs. Its structure allows for interactions with biological systems, making it of interest in medicinal chemistry. Additionally, it may exhibit properties such as analgesic or anti-inflammatory effects, similar to other compounds in its class. Safety data indicates that, like many amines, it should be handled with care due to potential irritant effects on skin and mucous membranes. Overall, 2-(4-aminophenyl)acetamide is a compound of significant interest in both research and industrial applications.

Formula: C₈H₁₀N₂O

InChI: InChI=1/C8H10N2O/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4H,5,9H2,(H2,10,11)

SMILES: c1cc(ccc1CC(=N)O)N

Synonyms:

• 4-Amino-benzeneacetamide
• BENZENEACETAMIDE, 4-AMINO-
• Benzeneacetamide, 4-amino- (9CI)

Benzeneacetamide, 4-amino- (9CI)

CAS: 6633-76-7

Formula: C₈H₁₀N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 150.1778

Ref: IN-DA00FJDC

2-(4-Aminophenyl)acetamide

CAS: 6633-76-7

2-(4-Aminophenyl)acetamide

Purity: 97%

Molecular weight: 150.18g/mol

Ref: 54-OR75983

2-(4-AMINOPHENYL)ACETAMIDE

CAS: 6633-76-7

Formula: C₈H₁₀N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 150.181

Ref: 10-F305578

2-(4-Aminophenyl)acetamide

CAS: 6633-76-7

2-(4-Aminophenyl)acetamide is a white crystalline solid with a melting point of 146°C. It has the optical rotation of +232° and 13c-nmr spectroscopy in DMSO-d6, with chemical shifts at δ = 9.3 (1H), 8.8 (1H), 7.5 (2H), 5.9 (1H), 5.8 (1H). 2-(4-Aminophenyl)acetamide has been synthesized from 4-aminobenzenesulfonyl chloride and 2-methylacetic acid in the presence of triethylamine and potassium carbonate as catalysts. This compound has two conformations, one being lamellar and the other being switchable between lamellar and non-lamellar structures due to its amide linkage. In addition, this compound can be used to study bacterial cell wall biosynthesis by using microscopy

Formula: C₈H₁₀N₂O

Purity: Min. 95%

Molecular weight: 150.18 g/mol

Ref: 3D-GAA63376