CAS 700-63-0
:2-Amino-2-phenylacetamide
Description:
2-Amino-2-phenylacetamide, with the CAS number 700-63-0, is an organic compound characterized by the presence of both an amino group and an acetamide functional group. This compound features a phenyl group attached to the carbon adjacent to the amino group, which contributes to its aromatic properties. It is typically a white to off-white solid at room temperature and is soluble in polar solvents such as water and alcohols, owing to the presence of the amino and amide functionalities. The compound exhibits basic properties due to the amino group, allowing it to participate in various chemical reactions, including acylation and amidation. It may also serve as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, 2-amino-2-phenylacetamide can exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C8H10N2O
InChI:InChI=1S/C8H10N2O/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H2,10,11)
InChI key:InChIKey=KIYRSYYOVDHSPG-UHFFFAOYSA-N
SMILES:C(C(N)=O)(N)C1=CC=CC=C1
Synonyms:- (±)-α-Aminobenzeneacetamide
- <span class="text-smallcaps">DL</span>-Phenylglycinamide
- <span class="text-smallcaps">DL</span>-Phenylglycine amide
- <span class="text-smallcaps">DL</span>-α-Phenylglycine amide
- Acetamide, 2-amino-2-phenyl-
- Benzeneacetamide, alpha-amino-
- Benzeneacetamide, α-amino-
- Brn 0972472
- Nsc 47695
- α-Amino-α-phenylacetamide
- 2-Amino-2-phenylacetamide
- See more synonyms
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Found 5 products.
2-Amino-2-phenylacetamide
CAS:Formula:C8H10N2OPurity:98%Color and Shape:SolidMolecular weight:150.1778DL-2-Phenylglycinamide
CAS:Controlled ProductFormula:C8H10N2OColor and Shape:NeatMolecular weight:150.182-Amino-2-phenylacetamide
CAS:<p>2-Amino-2-phenylacetamide is a model compound that has been used to study enzyme catalysis. It is an amide with a hydroxylamine group and an aromatic ring. 2-Amino-2-phenylacetamide inhibits the replication of DNA by binding to the protein polymerase, which blocks the transfer of amino acids from the tRNA molecule to the growing strand of DNA. This leads to apoptosis in cells that are susceptible to this type of inhibition. The synthesis of 2-Amino-2-phenylacetamide can be achieved through two methods: nitration of phenylacetic acid and oxidation of benzoic acid with nitric acid. Hydrochloric acid is required for both methods, as well as zinc chloride for the nitration method.<br>2-Amino-2-phenylacetamide is also known as succinoyl.</p>Formula:C8H10N2OPurity:Min. 95%Molecular weight:150.18 g/mol




