958635-18-2 Usage
Description
(8aS)-Tetrahydro-3-oxo-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxylic acid 1,1-dimethylethyl ester is a complex chemical compound that is an ester derivative of (8aS)-Tetrahydro-3-oxo-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxylic acid, a carboxylic acid. The presence of the 1,1-dimethylethyl ester group suggests that it may be used as a drug or pharmaceutical intermediate. Its molecular formula and molecular weight indicate that it is a relatively small molecule, and further research and analysis are needed to determine its potential applications and properties.
Uses
Used in Pharmaceutical Industry:
(8aS)-Tetrahydro-3-oxo-3H-oxazolo[3,4-a]pyrazine-7(1H)-carboxylic acid 1,1-dimethylethyl ester is used as a drug or pharmaceutical intermediate for its potential therapeutic properties. Its complex structure and ester derivative nature may contribute to its efficacy in treating various medical conditions, although further research is required to confirm its specific applications and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 958635-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,6,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 958635-18:
(8*9)+(7*5)+(6*8)+(5*6)+(4*3)+(3*5)+(2*1)+(1*8)=222
222 % 10 = 2
So 958635-18-2 is a valid CAS Registry Number.
958635-18-2Relevant articles and documents
A practical synthesis of differentially protected 2-(Hydroxymethyl) piperazines
Gao, Hongwu,Renslo, Adam R.
, p. 8591 - 8592 (2007)
(Chemical Equation Presented) An efficient and scalable synthesis of three differentially protected 2-(hydroxymefhyl)piperazines is presented, starting from optically active and commercially available (2S)-piperazine-2-carboxylic acid dihydrochloride. These synthetic building blocks are useful in the preparation of biologically active compounds and as chemical scaffolds for the construction of combinatorial libraries.