92085-96-6 Usage
Uses
Used in Organic Synthesis:
ERYTHRO-N-BOC-O-BENZYL-L-SERINE EPOXIDE serves as a crucial intermediate in organic synthesis, where it is used as a building block for constructing more complex organic molecules. Its presence of a Boc protecting group and a benzyl ester group allows for selective reactions and the formation of a diverse range of compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, ERYTHRO-N-BOC-O-BENZYL-L-SERINE EPOXIDE is employed as a precursor for the synthesis of pharmaceuticals. Its unique structure and functional groups enable the development of new drugs with potential therapeutic applications.
Used in the Preparation of Bioactive Molecules:
ERYTHRO-N-BOC-O-BENZYL-L-SERINE EPOXIDE is also utilized in the preparation of bioactive molecules, which have the potential to interact with biological systems and exhibit pharmacological effects. The epoxide group in particular can be involved in various chemical reactions that lead to the formation of biologically active compounds.
Used in Pharmaceutical Development:
ERYTHRO-N-BOC-O-BENZYL-L-SERINE EPOXIDE plays a significant role in pharmaceutical development, where it is used as a key component in the synthesis of new drugs. Its reactivity and structural features make it a valuable asset in the design and creation of innovative therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 92085-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,8 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92085-96:
(7*9)+(6*2)+(5*0)+(4*8)+(3*5)+(2*9)+(1*6)=146
146 % 10 = 6
So 92085-96-6 is a valid CAS Registry Number.
92085-96-6Relevant academic research and scientific papers
FunctionaIized erythro N-protected α-amino epoxides. Stereocontrolled synthesis and biological activity
Albeck, Amnon,Estreicher, Gary I.
, p. 5325 - 5338 (2007/10/03)
Erythro N-protected α-amino epoxides, derived from α-amino acids bearing functionalized side chains, were synthesized. The key synthetic step is a stereoselective reduction of the corresponding haloketone either to the halohydrin or directly to the epoxid
SYNTHESIS OF (+)-GALANTINIC ACID, A CONSTITUENT AMINO ACID IN THE PEPTIDE ANTIBIOTIC GALANTIN I, via THE STEREOSELECTIVE EPOXIDATION OF A CHIRAL SERINE EQUIVALENT
Ohfune, Yasufumi,Kurokawa, Natsuko
, p. 1587 - 1590 (2007/10/02)
Epoxidation of (2R)-t-butoxycarbonylamino-3-butenol afforded, in a highly stereoselective manner, a threo-3,4-epoxy-2-aminobutanol derivative which was succesfully converted to the unusual amino acid (+)-galantinic acid in 8 steps via regiospecific epoxide ring opening with divinyl cuprate.
