333319-62-3 Usage
Compound Formation
1-Phenylethylamine oxalamic acid ethyl ester is a compound formed by the reaction of 1-phenylethylamine with oxalamic acid and ethyl ester.
Uses
It is used as a precursor in the synthesis of various organic compounds and pharmaceuticals.
Potential Applications
It has potential applications in medicinal chemistry and drug development due to its diverse reactivity and functional groups.
Building Block
It may be used as a building block in the synthesis of other complex molecules.
Starting Material
It can serve as a starting material for the production of new chemical entities with potential therapeutic properties.
Unique Structure
Its unique structure and chemical properties make it a valuable intermediate in organic synthesis and medicinal research.
Check Digit Verification of cas no
The CAS Registry Mumber 333319-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,1 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 333319-62:
(8*3)+(7*3)+(6*3)+(5*3)+(4*1)+(3*9)+(2*6)+(1*2)=123
123 % 10 = 3
So 333319-62-3 is a valid CAS Registry Number.
333319-62-3Relevant articles and documents
Visible-light mediated carbamoyl radical addition to heteroarenes
Jatoi, Ashique Hussain,Pawar, Govind Goroba,Robert, Frédéric,Landais, Yannick
supporting information, p. 466 - 469 (2019/01/10)
The generation of carbamoyl radicals, followed by their addition to heteroarenes, was performed under mild conditions through a metal-free photocatalyzed decarboxylation of oxamic acids. The process has been applied to the carbamoylation of heteroaromatic bases using α-aminoacid-derived oxamic acids, leading to the corresponding amides without racemization.
N-Boc ethyl oxamate: A new nitrogen nucleophile for use in Mitsunobu reactions
Berree, Fabienne,Michelot, Gwendal,Le Corre, Maurice
, p. 8275 - 8276 (2007/10/03)
N-Boc ethyl oxamate can be directly coupled with primary and secondary alcohols under Mitsunobu conditions to afford various N-Boc mines after mild deprotection.
