55677-60-6

Basic information

• Product Name: 2-Amino-N-phenethylacetamide hydrochloride
• Synonyms: 2-Amino-N-phenethylacetamide hydrochloride;2-amino-N-(2-phenylethyl)acetamide hydrochloride
• CAS NO: 55677-60-6
• Molecular Formula: C₁₀H₁₄N₂O*ClH
• Molecular Weight: 214.7
• Mol File: 55677-60-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Amino-N-phenethylacetamide hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-N-phenethylacetamide hydrochloride(55677-60-6)
• EPA Substance Registry System: 2-Amino-N-phenethylacetamide hydrochloride(55677-60-6)

Safety Data

• Hazardous Substances Data: 55677-60-6(Hazardous Substances Data)

Usage

General Description

2-Amino-N-phenethylacetamide hydrochloride is a chemical compound that consists of an amino group and a phenethylacetamide group, with a hydrochloride salt. It is used in pharmaceutical and research applications as a reagent or precursor in the synthesis of various compounds. 2-Amino-N-phenethylacetamide hydrochloride has potential therapeutic properties and has been studied for its potential use in the treatment of central nervous system disorders. Additionally, it may have applications in the development of new drugs or as a research tool in neuroscience and pharmacology. Overall, 2-Amino-N-phenethylacetamide hydrochloride is a versatile chemical with potential medical and scientific applications.

Upstream product

• 55677-50-4 (Phenethylcarbamoyl-methyl)-carbamic acid benzyl ester 
• 613675-75-5 tert-butyl N-{[(2-phenylethyl)carbamoyl]methyl}carbamate 
• 64-04-0 phenethylamine 

Downstream Products

• 208665-25-2 N-<<1-<(benzyloxycarbonyl)amino>-2-phenylethyl>-methoxyphosphinyl>-glycyl-2-phenylethylamine 
• 315249-56-0 (R)-5-Guanidino-2-phenylmethanesulfonylamino-pentanoic acid ({(S)-1-benzyl-2-hydroxy-2-[(phenethylcarbamoyl-methyl)-carbamoyl]-ethylcarbamoyl}-methyl)-methyl-amide 
• 749838-42-4 C₃₆H₄₇N₉O₉S 

Relevant articles and documents

Asymmetric Disulfanylbenzamides as Irreversible and Selective Inhibitors of Staphylococcus aureus Sortase A

Staphylococcus aureus is one of the most frequent causes of nosocomial and community-acquired infections, with drug-resistant strains being responsible for tens of thousands of deaths per year. S. aureus sortase A inhibitors are designed to interfere with

Synthesis and Evaluation of 1- and 2-Substituted Fentanyl Analogues for Opioid Activity

We synthesized fentanyl analogues that posses key groups common to the opioid peptides to investigate whether or not these two classes of compounds interact with common subsites on opioid receptors.The design of the analogues was based on the possibility of structural analogy between the two aromatic rings of fentanyl and the Tyr1 and Phe4 residues of the opioid peptides.The synthesized compounds showed very week or no opioid activity as tested in the electrically stimulated longitudinal muscle of the guinea pig ileum or mouse vas deferens preparations.These results, together with those of reported studies, suggest that fentanyl and the opioid peptides interact with diffrent subsites on either μ or δ receptors.Studies using the irreversible μ opioid receptor antagonist, β-funaltrexamine, indicate that fentanyl interacts preferentially with μ opioid receptors.