147700-91-2 Usage
Uses
Used in Organic Synthesis:
(5S)-3,4,5,6-TETRAHYDRO-5-PHENYL-N-(BENZYLOXYCARBONYL)-4(H)-1,4-OXAZIN-2-ONE is used as a building block for the synthesis of various organic compounds, due to its versatile intermediate properties.
Used in Medicinal Chemistry:
(5S)-3,4,5,6-TETRAHYDRO-5-PHENYL-N-(BENZYLOXYCARBONYL)-4(H)-1,4-OXAZIN-2-ONE is used as a versatile intermediate for the preparation of bioactive molecules in medicinal chemistry.
Used in Pharmaceutical Development:
(5S)-3,4,5,6-TETRAHYDRO-5-PHENYL-N-(BENZYLOXYCARBONYL)-4(H)-1,4-OXAZIN-2-ONE is used as a valuable tool for researchers in the development of new pharmaceuticals, due to its potential as a versatile intermediate.
Used in Agrochemical Development:
(5S)-3,4,5,6-TETRAHYDRO-5-PHENYL-N-(BENZYLOXYCARBONYL)-4(H)-1,4-OXAZIN-2-ONE is used as a valuable tool for researchers in the development of new agrochemicals, due to its potential as a versatile intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 147700-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,0 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147700-91:
(8*1)+(7*4)+(6*7)+(5*7)+(4*0)+(3*0)+(2*9)+(1*1)=132
132 % 10 = 2
So 147700-91-2 is a valid CAS Registry Number.
147700-91-2Relevant academic research and scientific papers
Highly diastereoselective alkylation of the Dellaria oxazinone template with bifunctional electrophiles
Roos, Gregory H. P.,Dastlik, Kim A.
, p. 2197 - 2208 (2007/10/03)
This study investigates the efficiency of alkylation of the Dellaria oxazinone glycinate template with sensitive bifunctional electrophiles. In addition to improved access to the template, triflate/halide bifunctional combinations provided good yields (85-93%) of highly diastereoselective alkylation products.
An expedient route to the glycine templates (R)- or (S)-N-Cbz-5-phenyl-1,4-oxazin-2-one
Dastlik, Kim A.,Giles, Robin G.F.,Roos, Gregory H.P.
, p. 2525 - 2526 (2007/10/03)
An economical and practical route to the title compounds is described. The three step, essentially 'one pot' sequence proceeds in overall yields of up to 80% without the need for chromatography of intermediate isolation.
