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(R)-3-(benzyloxycarbonyl)-4-isopropyl-[1,2,3]oxathiazolidine 2,2-dioxide is a complex organic compound characterized by a central oxathiazolidine ring, to which a benzyloxycarbonyl group and an isopropyl group are attached. This molecular structure endows it with potential for interaction with biological systems, making it a candidate for pharmaceutical research and development. Furthermore, its chiral nature suggests it could serve as a valuable building block in organic synthesis.

1007121-73-4

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1007121-73-4 Usage

Uses

Used in Pharmaceutical Research and Development:
(R)-3-(benzyloxycarbonyl)-4-isopropyl-[1,2,3]oxathiazolidine 2,2-dioxide is used as a potential candidate in pharmaceutical research and development due to its structural features that allow for interactions with biological systems. Its unique molecular composition may contribute to the development of new drugs or therapeutic agents.
Used as a Chiral Building Block in Organic Synthesis:
In the field of organic chemistry, (R)-3-(benzyloxycarbonyl)-4-isopropyl-[1,2,3]oxathiazolidine 2,2-dioxide is used as a chiral building block. Its specific stereochemistry can be leveraged to create a variety of complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1007121-73-4 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 1007121-73:
(9*1)+(8*0)+(7*0)+(6*7)+(5*1)+(4*2)+(3*1)+(2*7)+(1*3)=84
84 % 10 = 4
So 1007121-73-4 is a valid CAS Registry Number.

1007121-73-4Relevant academic research and scientific papers

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

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