1007121-75-6 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-(benzyloxycarbonyl)-4-benzyl-[1,2,3]oxathiazolidine 2,2-dioxide is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the development of new drugs and chemical entities with diverse biological activities.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-3-(benzyloxycarbonyl)-4-benzyl-[1,2,3]oxathiazolidine 2,2-dioxide serves as a key building block. Its heterocyclic structure allows for the creation of new chemical entities with a wide range of biological activities, contributing to the advancement of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1007121-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,1,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1007121-75:
(9*1)+(8*0)+(7*0)+(6*7)+(5*1)+(4*2)+(3*1)+(2*7)+(1*5)=86
86 % 10 = 6
So 1007121-75-6 is a valid CAS Registry Number.
1007121-75-6Relevant academic research and scientific papers
Modular, gold-catalyzed approach to the synthesis of lead-like piperazine scaffolds
James, Thomas,Simpson, Iain,Grant, J. Andrew,Sridharan, Visuvanathar,Nelson, Adam
, p. 6094 - 6097 (2014/01/06)
Ring-opening of cyclic sulfamidates with propargylic sulfonamides yielded substrates for a gold-catalyzed cyclization to yield tetrahydropyrazines. Manipulation of the tetrahydropyrazines, by reduction or using multicomponent reactions, yielded piperazine scaffolds in which substitution of the carbon atoms was varied. Such scaffolds may have value in the synthesis of novel screening compounds with lead-like molecular properties.
Synthesis of 2,6-disubstituted piperazines by a diastereoselective palladium-catalyzed hydroamination reaction
Cochran, Brian M.,Michael, Forrest E.
, p. 329 - 332 (2008/09/19)
(Chemical Equation Presented) A highly diastereoselective intramolecular hydroamination is the key step in a modular synthesis of 2,6-disubstituted piperazines. The requisite hydroamination substrates were prepared in excellent yields by nucleophilic disp
