13023-70-6 Usage
Description
Pentanamide, 5-amino-, also known as 5-aminopentanoic amide, is a fatty amide consisting of pentanamide with an amino substituent at the 5-position. It is a derivative of pentanamide, which is a saturated fatty acid amide with a five-carbon chain. The presence of the amino group at the 5-position provides unique chemical and biological properties, making it a versatile compound for various applications.
Uses
Used in Pharmaceutical Industry:
Pentanamide, 5-amino-, is used as a pharmaceutical intermediate for the synthesis of various drugs and drug candidates. The presence of the amino group allows for the formation of amide bonds with other molecules, facilitating the development of new drug entities with potential therapeutic applications.
Used in Chemical Synthesis:
Pentanamide, 5-amino-, is used as a building block in the synthesis of various organic compounds, including peptides, polymers, and other bioactive molecules. The amino group can be used for further functionalization, enabling the creation of diverse chemical structures with specific properties and applications.
Used in Research and Development:
Pentanamide, 5-amino-, is used as a research tool in the study of biological processes and the development of new therapeutic agents. Its unique structure allows researchers to investigate its interactions with biological targets, such as enzymes, receptors, and other macromolecules, providing insights into its potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 13023-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13023-70:
(7*1)+(6*3)+(5*0)+(4*2)+(3*3)+(2*7)+(1*0)=56
56 % 10 = 6
So 13023-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O/c6-4-2-1-3-5(7)8/h1-4,6H2,(H2,7,8)
13023-70-6Relevant articles and documents
A Critical Test of the Theory of Stereoelectronic Control
Perrin, Charles L.,Arrhenius, Gloria Meichia L.
, p. 2839 - 2842 (1982)
According to Deslongchamps' theory of stereoelectronic control, preferential cleavage of a tetrahedral intermediate occurs when there are two lone pairs antiperiplanar to the leaving group.However, it is concluded that the experimental evidence is ambiguous, because it requires an unreasonable assumption regarding rates of ring inversion and because there is a simpler explanation for the observations.Nevertheless, the theory is a plausible one, deserving unambiguous evidence to support it.The hydrolysis of cyclic amidines (4), via the hemiorthoamide (5), can provide a suitable test.It is observed that 2-amino-1-pyrroline (4, n = 5) and "2-iminopiperidine" (4, n = 6) hydrolyze in base solely to the amino amide (6), which is converted under the reaction conditions to the thermodynamically more stable lactam (7).This result is the first unambiguous evidence for stereoelectronic control, and it also shows that cleavage of the intermediate (5) is fast compared to nitrogen inversion.
Compounds having growth hormone releasing activity
-
, (2008/06/13)
Compounds that promote growth hormone releasing activity are disclosed. These compounds have the formula: A1-A2-X; A1-X′; or A1.-Y These compounds can be present in a pharmaceutical composition. The compounds can be used with a second compound that acts as an agonist at the growth hormone releasing hormone receptor or which inhibits the effects of somatostatin. These compounds can be used for a variety of uses such as treating hypothalamic pituitary dwarfism, osteoporosis, burns, or promoting wound healing.