306773-85-3 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-benzyloxycarbonylamino-4-tert-butoxycarbonylamino-2-oxazolidone is used as a chiral building block for the synthesis of pharmaceuticals and biologically active molecules. Its ability to act as a versatile and selective catalyst in various chemical reactions makes it a valuable tool in drug discovery and development.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-3-benzyloxycarbonylamino-4-tert-butoxycarbonylamino-2-oxazolidone is utilized as a key component for the preparation of complex molecules with high enantioselectivity and purity. The presence of Boc and Cbz protecting groups in the molecule allows for the protection of specific functional groups during chemical reactions, which can be removed under specific conditions to reveal the original functional groups, enhancing the compound's utility in synthetic processes.
Used in Catalyst Development:
(S)-3-benzyloxycarbonylamino-4-tert-butoxycarbonylamino-2-oxazolidone is employed as a catalyst in a variety of chemical reactions due to its versatility and selectivity. This property makes it an essential component in the development of new and improved catalysts for various applications in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 306773-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,7,7 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 306773-85:
(8*3)+(7*0)+(6*6)+(5*7)+(4*7)+(3*3)+(2*8)+(1*5)=153
153 % 10 = 3
So 306773-85-3 is a valid CAS Registry Number.
306773-85-3Relevant academic research and scientific papers
Sypniewski, Michal,Penke, Botond,Simon, Lajos,Rivier, Jean
, p. 6595 - 6600 (2000)
The enantiospecific synthesis of (R)-Boc-(Fmoc)-aminoglycine 7 was achieved. (S)-Cbz-serine 1 was reacted with diphenylphosphoryl azide in the presence of triethylamine to yield cyclic(S) carbamate 2. The ring nitrogen of 2 was protected with a Boc group.
