7355-37-5 Usage
Description
(4E)-4-[(hexylamino)methylidene]-5-(hydroxymethyl)-2-methylpyridin-3(4H)-one is a pyridinone derivative featuring a hexylamino group attached to a methylidene bridge. (4E)-4-[(hexylamino)methylidene]-5-(hydroxymethyl)-2-methylpyridin-3(4H)-one also contains a hydroxymethyl group and a methyl group on the pyridinone ring. Its structural features, such as the presence of an amino group and a hydroxymethyl group, suggest potential pharmaceutical or biological applications. Further research could uncover its significance in fields like medicinal chemistry and pharmacology.
Uses
Used in Pharmaceutical Industry:
(4E)-4-[(hexylamino)methylidene]-5-(hydroxymethyl)-2-methylpyridin-3(4H)-one is used as a potential pharmaceutical candidate for various applications due to its structural features that may allow for interactions with biological systems.
Used in Medicinal Chemistry:
(4E)-4-[(hexylamino)methylidene]-5-(hydroxymethyl)-2-methylpyridin-3(4H)-one is used as a compound of interest in medicinal chemistry for its potential to be developed into new drugs or therapeutic agents, given its unique structural components.
Used in Biological Research:
(4E)-4-[(hexylamino)methylidene]-5-(hydroxymethyl)-2-methylpyridin-3(4H)-one is used as a subject of study in biological research to explore its interactions with biological systems and to understand its potential applications in the life sciences.
Check Digit Verification of cas no
The CAS Registry Mumber 7355-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7355-37:
(6*7)+(5*3)+(4*5)+(3*5)+(2*3)+(1*7)=105
105 % 10 = 5
So 7355-37-5 is a valid CAS Registry Number.
7355-37-5Relevant articles and documents
Kinetic study of the reaction between some compounds of the vitamin B-6 group and n-hexylamine
Vazquez, M. A.,Donoso, J.,Munoz, F.,Blanco, F. Garcia,Vado, M. A. Garcia Del,Echevarria, G.
, p. 361 - 363 (2007/10/02)
Schiff's base formation between pyridoxal and 5'-deoxypyridoxal and n-hexylamine has been investigated as a function of pH at 25 deg C and 0.1 ionic strength.These results are compared with those obtained for the Schiff's base from pyridoxal 5'-phosphate and n-hexylamine.The protonation constants as well as the microscopic kinetic and equilibrium constants for the ionic species in solution were determined.We have assumed that the slow step for this reaction is the loss of H2O from the carbinolamine to yield the imine.Our results indicate that all the protonatable groups of the molecule are involved in intramolecular acid catalysis of the dehydration of the carbinolamine, although the efficiency of this intramolecular catalysis is not affected by the presence of the phosphate group of the aldehyde.
