85147-15-5 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 2-hydroxy-5-Methylnicotinate is used as an active pharmaceutical ingredient for its anti-inflammatory and antioxidant properties, contributing to the development of drugs that address various health conditions.
Used in Cosmetic Industry:
In the cosmetic sector, Ethyl 2-hydroxy-5-Methylnicotinate serves as a key component in skincare products, leveraging its anti-inflammatory and antioxidant characteristics to improve skin health and appearance.
Used in Food Industry:
Ethyl 2-hydroxy-5-Methylnicotinate is utilized as a flavoring agent, imparting a pleasant and fruity taste to a range of food products, thereby enhancing their sensory appeal.
Used in Cardiovascular Health Research:
Ethyl 2-hydroxy-5-Methylnicotinate is studied for its potential benefits in the treatment of cardiovascular diseases, capitalizing on its ability to improve blood circulation and support heart health.
Check Digit Verification of cas no
The CAS Registry Mumber 85147-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85147-15:
(7*8)+(6*5)+(5*1)+(4*4)+(3*7)+(2*1)+(1*5)=135
135 % 10 = 5
So 85147-15-5 is a valid CAS Registry Number.
85147-15-5Relevant academic research and scientific papers
An Alternate Synthesis of 6-Substituted-5-deazapteridines
DeGraw, Joseph I.,Tagawa, Hiroaki
, p. 1461 - 1463 (2007/10/02)
A procedure for synthesis of 2,4-diamino-6-substituted-5-deazapteridines (pyridopyrimidines) is described.Condensation of 1-piperidino-1-propene with ethoxymethylenemalononitrile afforded an enamino malononitrile adduct, which then treated with ammonia yielded 2-amino-3-cyano-5-methylpyridine.Cyclization to 2,4-diamino-6-methyl-5-diazapteridine could be effected with guanidine.Similar condensation of piperidinopropene with ethyl methoxymethylenecyanoacetate followed by cyclization with hydroxylamine gave 2-amino-3-carbethoxy-6-methylpyridine 1-oxide.Reduction with phosphorus trichloride afforded the pyridine base, however, attempts to cyclize the amino ester to 2-amino-4-hydroxy-6-methyl-5-deazapteridine were unsuccessful.
