579467-28-0 Usage
Description
(3R,8aS)-rel-Hexahydro-3-(hydroxyMethyl)-8a-Methyl-5-oxo-7H-oxazolo[3,2-a]pyrazine-7-carboxylic acid phenylMethyl ester is a complex organic molecule characterized by its hexahydro-3-(hydroxyMethyl)-8a-Methyl-5-oxo-7H-oxazolo[3,2-a]pyrazine-7-carboxylic acid core and a phenylMethyl ester group. (3R,8aS)-rel-Hexahydro-3-(hydroxyMethyl)-8a-Methyl-5-oxo-7H-oxazolo[3,2-a]pyrazine-7-carboxylic acid phenylMethyl ester features a cyclic structure with a carboxylic acid functional group, which may contribute to its potential pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
(3R,8aS)-rel-Hexahydro-3-(hydroxyMethyl)-8a-Methyl-5-oxo-7H-oxazolo[3,2-a]pyrazine-7-carboxylic acid phenylMethyl ester is used as a potential pharmaceutical candidate for various applications due to its complex structure and the presence of a carboxylic acid group, which can be important for drug delivery and formulation.
Used in Drug Delivery Systems:
In the field of drug delivery, (3R,8aS)-rel-Hexahydro-3-(hydroxyMethyl)-8a-Methyl-5-oxo-7H-oxazolo[3,2-a]pyrazine-7-carboxylic acid phenylMethyl ester may be utilized to enhance the delivery, bioavailability, and therapeutic outcomes of certain drugs. Its carboxylic acid group could potentially facilitate interactions with other molecules or drug carriers, improving the overall effectiveness of the treatment.
Further research and testing are necessary to determine the specific pharmacological and biological properties of this chemical, as well as its suitability for various applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 579467-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,9,4,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 579467-28:
(8*5)+(7*7)+(6*9)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=220
220 % 10 = 0
So 579467-28-0 is a valid CAS Registry Number.
579467-28-0Relevant articles and documents
Efficient, stereoselective synthesis of oxazolo[3,2-a]pyrazin-5-ones: Novel bicyclic lactam scaffolds from the bicyclocondensation of 3-aza-1,5-ketoacids and amino alcohols
Bencsik, Josef R.,Kercher, Timothy,O'Sullivan, Michael,Josey, John A.
, p. 2727 - 2730 (2007/10/03)
(Matrix presented) The bicyclocondensation of 3-aza-1,5-ketoacids and amino alcohols furnished novel oxazolo[3,2-a]pyrazin-5-one scaffolds possessing angular, ring junction substituents in high yield with excellent levels of substrate-based diastereocontr
