CAS 10268-06-1

Benzeneacetamide, 2-chloro-

Description:

Benzeneacetamide, 2-chloro- is an organic compound characterized by the presence of a benzene ring substituted with an acetamide group and a chlorine atom at the second position. This compound typically appears as a white to off-white solid and is known for its moderate solubility in organic solvents. The presence of the chloro substituent can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Benzeneacetamide derivatives are often studied for their biological activities, including potential pharmaceutical applications. The compound's molecular structure contributes to its properties, such as melting point, boiling point, and stability under different conditions. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, benzeneacetamide, 2-chloro- serves as an important compound in organic synthesis and medicinal chemistry, warranting further investigation into its applications and effects.

Formula: C₈H₈ClNO

Benzeneacetamide, 2-chloro-

CAS: 10268-06-1

Formula: C₈H₈ClNO

Purity: 97%

Color and Shape: Solid

Molecular weight: 169.6082

Ref: IN-DA00083Q

2-(2-Chlorophenyl)acetamide

CAS: 10268-06-1

2-(2-Chlorophenyl)acetamide

Purity: 98%

Molecular weight: 169.61g/mol

Ref: 54-OR953412

2-(2-chlorophenyl)acetamide

CAS: 10268-06-1

Formula: C₈H₈ClNO

Purity: 97%

Color and Shape: Solid

Molecular weight: 169.61

Ref: 10-F357832

2-(2-Chlorophenyl)acetamide

CAS: 10268-06-1

2-(2-Chlorophenyl)acetamide is a trisubstituted acetamide that has been shown to bind to the benzodiazepine receptor. This binding prevents the binding of GABA to the receptor and inhibits the ion channel, which leads to increased cell membrane permeability and cell death. 2-(2-Chlorophenyl)acetamide also binds to the anhydrase II isoform, which causes inhibition of carbonic anhydrase activity. This in turn leads to increased levels of carbon dioxide in some tissues, such as those found in the eye, leading to irritation and pain. The compound has also been shown to inhibit mitogen-activated protein kinase (MAPK), which is a protein involved in cellular signalling pathways that regulate growth and differentiation. It does this by preventing phosphorylation of MAPK at tyrosine residues.

Formula: C₈H₈ClNO

Purity: Min. 95%

Molecular weight: 169.61 g/mol

Ref: 3D-KAA26806