113118-69-7 Usage
Uses
Used in Pharmaceutical Industry:
1(2H)-Pyridinecarboxylic acid, 3-methyl-, phenyl ester is used as a vasodilator for improving blood circulation. Its increased blood flow capabilities contribute to its use in topical preparations aimed at enhancing the appearance of the skin.
Used in Cosmetic Industry:
In the cosmetic industry, 1(2H)-Pyridinecarboxylic acid, 3-methyl-, phenyl ester is used as a skin conditioning agent. Its ability to improve blood circulation leads to better nutrient delivery and waste removal from the skin, resulting in a more youthful and healthy appearance.
Used in Dermatological Treatments:
1(2H)-Pyridinecarboxylic acid, 3-methyl-, phenyl ester is also being investigated for its potential use in dermatological treatments. It has shown promise in addressing conditions such as psoriasis and eczema, where improved blood circulation and skin conditioning can be beneficial for managing symptoms and promoting skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 113118-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,1 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113118-69:
(8*1)+(7*1)+(6*3)+(5*1)+(4*1)+(3*8)+(2*6)+(1*9)=87
87 % 10 = 7
So 113118-69-7 is a valid CAS Registry Number.
113118-69-7Relevant academic research and scientific papers
Enantioselective Diels-Alder reaction of 1,2-dihydropyridines with aldehydes using β-amino alcohol organocatalyst
Kohari, Yoshihito,Okuyama, Yuko,Kwon, Eunsang,Furuyama, Taniyuki,Kobayashi, Nagao,Otuki, Teppei,Kumagai, Jun,Seki, Chigusa,Uwai, Koji,Dai, Gang,Iwasa, Tatsuo,Nakano, Hiroto
, p. 9500 - 9511 (2015/01/09)
(Chemical Equation Presented) The enantioselective Diels-Alder reaction of 1,2-dihydropyridines with aldehydes using an easily prepared optically active β-amino alcohol catalyst was found to provide optically active isoquinuclidines, an efficient syntheti
SYNTHESIS OF SUBSTITUTED 3-PYRIDINECARBOXALDEHYDES
Comins, Daniel L.,Herrick, James J.
, p. 2159 - 2164 (2007/10/02)
Treatment of 3-substituted 1-(phenoxycarbonyl)-1,2-dihydropyridines with Vilsmeier reagent (POCl3/DMF) gave 3-substituted 5-formyl-1-(phenoxycarbonyl)-1,2-dihydropyridines, which were aromatized with hot sulfur to provide 5-substituted 3-pyridinecarboxaldehydes. The formylation of 4-substituted 1-(phenoxycarbonyl)-1,4-dihydropyridines and subsequent aromatization gave 4-substituted 3-pyridinecarboxaldehydes.
