CAS 116433-53-5

2-Azido-N-(phenylmethyl)acetamide

Description:

2-Azido-N-(phenylmethyl)acetamide is an organic compound characterized by the presence of an azido group (-N3) and an acetamide functional group. It features a phenylmethyl substituent, which contributes to its aromatic properties. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents due to the presence of the amide group. Its azido functionality makes it a potential candidate for various chemical reactions, including click chemistry, where it can participate in cycloaddition reactions. The presence of the phenylmethyl group can influence its reactivity and stability, often enhancing the compound's lipophilicity. Safety considerations are important when handling this compound, as azides can be sensitive to heat and shock, potentially leading to explosive decomposition. Overall, 2-Azido-N-(phenylmethyl)acetamide is of interest in synthetic organic chemistry and materials science, particularly in the development of new functional materials and pharmaceuticals.

Formula: C₉H₁₀N₄O

InChI: InChI=1S/C9H10N4O/c10-13-12-7-9(14)11-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,14)

InChI key: InChIKey=IBJSSQSSMGVSGR-UHFFFAOYSA-N

SMILES: C(NC(CN=[N+]=[N-])=O)C1=CC=CC=C1

Synonyms:

• 2-Azido-N-(phenylmethyl)acetamide
• 2-Azido-N-benzylacetamide
• N-Benzyl-2-azidoacetamide
• Acetamide, 2-azido-N-(phenylmethyl)-

2-Azido-N-benzylacetamide

CAS: 116433-53-5

2-Azido-N-benzylacetamide (2ABA) is a strain that can be used in biochemistry, specifically for the study of amides. It has been shown to be chemically stable and has a number of strategies that can be employed. 2ABA is an amide with phenyl substituents that have functional groups such as azides and traceless. The hydrogen bond in 2ABA forms through the bond cleavage reaction rate and ligation, which are triggered by triggerable bonds.

Formula: C₉H₁₀N₄O

Purity: Min. 95%

Molecular weight: 190.2 g/mol

Ref: 3D-REA43353