207122-29-0 Usage
Uses
Used in Pharmaceutical Research:
(S)-tert-Butyl 1-(tert-butyldimethylsilyloxy)-3-phenylpropan-2-ylcarbamate is used as a building block for the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. Its versatility as a precursor allows for the development of complex molecules with potential therapeutic properties.
Used in Organic Chemistry Research:
In the field of organic chemistry, (S)-tert-Butyl 1-(tert-butyldimethylsilyloxy)-3-phenylpropan-2-ylcarbamate is used as an intermediate for the synthesis of bioactive compounds. The tert-butyldimethylsilyloxy group can be easily removed under mild conditions, making it a valuable and versatile intermediate for creating a wide range of organic molecules.
Used in Synthesis of Complex Molecules:
(S)-tert-Butyl 1-(tert-butyldimethylsilyloxy)-3-phenylpropan-2-ylcarbamate is used as a valuable precursor for the synthesis of complex molecules in various chemical industries. Its unique structure and the ease of removing the protecting group make it an ideal candidate for creating intricate molecular structures with specific functions and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 207122-29-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,1,2 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 207122-29:
(8*2)+(7*0)+(6*7)+(5*1)+(4*2)+(3*2)+(2*2)+(1*9)=90
90 % 10 = 0
So 207122-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H35NO3Si/c1-19(2,3)24-18(22)21-17(14-16-12-10-9-11-13-16)15-23-25(7,8)20(4,5)6/h9-13,17H,14-15H2,1-8H3,(H,21,22)
207122-29-0Relevant academic research and scientific papers
Highly regioselective opening of optically active N-Boc-2,3-aziridino alcohol derivatives with metal halides
Righi, Giuliana,Franchini, Tiziana,Bonini, Carlo
, p. 2385 - 2388 (2007/10/03)
Chiral 3-substituted N-Boc-2,3-aziridino alcohols are opened in a regio and stereoselective fashion by MgBr2; the obtained 3-bromo derivatives can be reduced and deprotected under mild conditions to the corresponding 1,2- amino alcohols.
