761460-04-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-tert-Butyl 3-(2-ethoxy-2-oxoethyl)morpholine-4-carboxylate is used as a key intermediate in the development of pharmaceuticals for the treatment of neurological disorders, cancer, and infectious diseases. Its unique structure allows for the creation of novel drug candidates that can potentially address unmet medical needs.
Used in Agrochemical Production:
In the agrochemical industry, (S)-tert-Butyl 3-(2-ethoxy-2-oxoethyl)morpholine-4-carboxylate is utilized as a building block for the synthesis of new agrochemicals, contributing to the development of more effective and environmentally friendly products for agricultural use.
Used in Organic Chemistry:
(S)-tert-Butyl 3-(2-ethoxy-2-oxoethyl)morpholine-4-carboxylate is employed as a valuable component in the synthesis of various organic compounds, broadening the scope of chemical reactions and products that can be achieved in organic chemistry research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 761460-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 761460-04:
(8*7)+(7*6)+(6*1)+(5*4)+(4*6)+(3*0)+(2*0)+(1*4)=152
152 % 10 = 2
So 761460-04-2 is a valid CAS Registry Number.
761460-04-2Relevant articles and documents
An efficient synthesis of chiral cyclic β-amino acids via asymmetric hydrogenation
Pousset, Cyrille,Callens, Roland,Marinetti, Angela,Larchevêque, Marc
, p. 2766 - 2770 (2007/10/03)
Cyclic β-amino acids, homoproline, homopipecolic acid and 3-carboxy-methylmorpholine were obtained in high enantiomeric excesses by transition metal-catalyzed asymmetric hydrogenation of cyclic β-acylamino-alkenoates. These compounds were synthesized by a
Enzymatic resolution of cyclic N-Boc protected β-aminoacids
Pousset, Cyrille,Callens, Roland,Haddad, Mansour,Larcheveque, Marc
, p. 3407 - 3412 (2007/10/03)
Methyl and ethyl esters of N-Boc homoproline, homopipecolic acid and 3-carboxymethyl-morpholine were kinetically resolved by hydrolysis catalysed by Burkholderia cepacia lipase to give the corresponding acids and residual esters in enantiomeric excesses better than 99% (E > 100).
