100516-59-4 Usage
Uses
Used in Organic Synthesis:
(3S,5S,6R)-4-(benzyloxycarbonyl)-3-butyl-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one is used as a key intermediate for the synthesis of various complex organic compounds due to its unique structural features and potential reactivity.
Used in Pharmaceutical Industry:
(3S,5S,6R)-4-(benzyloxycarbonyl)-3-butyl-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one is used as a building block for the development of novel pharmaceuticals, leveraging its intricate structure to create new drugs with specific therapeutic properties.
Used in Materials Science:
(3S,5S,6R)-4-(benzyloxycarbonyl)-3-butyl-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one is used as a component in the development of advanced materials, potentially contributing to the creation of materials with unique mechanical, electronic, or optical properties.
Further research and analysis are necessary to fully understand the properties and potential uses of (3S,5S,6R)-4-(benzyloxycarbonyl)-3-butyl-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one, as its complex structure and potential reactivity may offer a wide range of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 100516-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,1 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100516-59:
(8*1)+(7*0)+(6*0)+(5*5)+(4*1)+(3*6)+(2*5)+(1*9)=74
74 % 10 = 4
So 100516-59-4 is a valid CAS Registry Number.
100516-59-4Relevant academic research and scientific papers
Practical Asymmetric Syntheses of α-Amino Acids through Carbon-Carbon Bond Constructions on Electrophilic Glycine Templates
Williams, Robert M.,Sinclair, Peter J.,Zhai, Dongguan,Chen, Daimo
, p. 1547 - 1557 (2007/10/02)
The optically active D- and L-erythro-4-(benzyloxycarbonyl)-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-ones (3) and D- and L-erythro-4-(tert-butoxycarbonyl)-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-ones (3) can be efficiently brominated to serve as electrophilic glycine templates for the asymmetric synthesis of amino acids.It was found that coupling to these templates can proceed with either net retention or net inversion of stereochemistry.The final deblocking to the amino acids is accomplished with either dissolving-metal reduction or catalytic hydrogenolysis.The syntheses of β-ethyl aspartic acid, norvaline, allylglycine, alanine, norleucine, homophenylalanine, p-methoxyhomophenylalanine, cyclopentylglycine, and cyclopentenylglycine and a formal synthesis of clavalanine are described.In addition, the direct asymmetric syntheses of N-t-BOC-allylglycine and N-t-BOC-cyclopentenylglycine are described.
