30057-76-2 Usage
Uses
Used in Pharmaceutical Research and Development:
N-(2-Oxoheptan-3-yl)acetamide is utilized as a key intermediate in the synthesis of novel pharmaceutical compounds, contributing to the advancement of drug discovery and development. Its unique structure allows for the creation of new molecules with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, N-(2-Oxoheptan-3-yl)acetamide is employed as a versatile building block for the assembly of complex organic molecules. Its reactivity and structural features facilitate the synthesis of a wide array of compounds with diverse applications.
Used in Chemical Intermediates Production:
N-(2-Oxoheptan-3-yl)acetamide serves as a precursor for the production of various chemical intermediates, which are essential in the manufacturing process of numerous industrial products, including specialty chemicals and materials.
Used in Research and Development of New Compounds:
Due to its unique chemical structure, N-(2-Oxoheptan-3-yl)acetamide is used in research and development to explore the synthesis of new compounds with potential applications in various industries, such as agriculture, materials science, and environmental technology.
Check Digit Verification of cas no
The CAS Registry Mumber 30057-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,5 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30057-76:
(7*3)+(6*0)+(5*0)+(4*5)+(3*7)+(2*7)+(1*6)=82
82 % 10 = 2
So 30057-76-2 is a valid CAS Registry Number.
30057-76-2Relevant academic research and scientific papers
New N6- or N(9)-hydroxyalkyl substituted 8-azaadenines or adenines as effective A1 adenosine receptor ligands.
Biagi, Giuliana,Giorgi, Irene,Leonardi, Michele,Livi, Oreste,Pacchini, Federica,Scartoni, Valerio,Costa, Barbara,Lucacchini, Antonio
, p. 801 - 810 (2007/10/03)
In this paper we describe synthesis and biological assays of some A(1) ligands more water-soluble than the effective, but very lipophilic, 8-azaadenines and adenines discovered in the past and obtained introducing on N(6) or N(9) substituent a hydroxy group. Five of the new N(6)-hydroxyalkyl- and N(6)-hydroxycycloalkyl-2-phenyl-9-benzyl-8-azaadenines showed very high affinity (Ki40 nM) and selectivity for A(1) adenosine receptors. Among the 2-phenyl-9-(2-hydroxy-3-alkyl)-8-azaadenines or adenines prepared, the compounds with the higher A(1) affinity and selectivity resulted 2-phenyl-9-(2-hydroxy-3-propyl)-N(6)-cyclopentyl- and cyclohexyl-8-azaadenine with Ki 2.2+/-0.2 nM and 2.8+/-0.3 nM respectively. From the point of view of water-solubility, 2-phenyl-9-(2-hydroxy-3-propyl)-8-azaadenine was the most interesting compound, having a CLogP of 1.066991 and a water-solubility of 1.2 mg mL(-1).
