76267-48-6 Usage
Uses
Used in Pharmaceutical Industry:
(1R,4aS,7S,7aS)-1-Hydroxy-7-hydroxymethyl-1,4a,5,6,7,7a-hexahydro-cyclopenta[c]pyran-4-carboxylic acid methyl ester is used as a potential pharmaceutical candidate due to its complex cyclic structure and functional groups. The hydroxy and carboxylic acid groups may allow for interactions with biopolymers and macromolecules, which could be harnessed for medicinal purposes.
Used in Chemical Synthesis:
(1R,4aS,7S,7aS)-1-Hydroxy-7-hydroxymethyl-1,4a,5,6,7,7a-hexahydro-cyclopenta[c]pyran-4-carboxylic acid methyl ester is used as a building block in the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable component in creating new compounds with specific properties and potential applications.
Further research and analysis are required to fully explore the properties and potential uses of (1R,4aS,7S,7aS)-1-Hydroxy-7-hydroxymethyl-1,4a,5,6,7,7a-hexahydro-cyclopenta[c]pyran-4-carboxylic acid methyl ester, including its pharmacological or biological activities and its role in the development of new drugs or materials.
Check Digit Verification of cas no
The CAS Registry Mumber 76267-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,6 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76267-48:
(7*7)+(6*6)+(5*2)+(4*6)+(3*7)+(2*4)+(1*8)=156
156 % 10 = 6
So 76267-48-6 is a valid CAS Registry Number.
76267-48-6Relevant academic research and scientific papers
THE PRACTICAL METHOD FOR THE PREPARATION OF IRIDOID AGLYCONS FROM THEIR GLYCOSIDES
Tanaka, Masahide,Kigawa, Masaharu,Mitsuhashi, Hiroshi,Wakamatsu, Takeshi
, p. 1451 - 1454 (2007/10/02)
The liberation of iridoid aglycons from their glycosides is achieved by the successive treatment with sodium metaperiodate, sodium borohydride, and hydrochloric acid in one pot operation.This simple and efficient method has advantages over the enzymatic hydrolysis from the preparative point of view.
