91613-84-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(ethoxycarbonylamino)-2-methyl-propanoic acid is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its properties and structure make it suitable for use in the development of pharmaceuticals, contributing to the creation of new and effective treatments.
Used in Organic Synthesis:
In the field of organic chemistry, 2-(ethoxycarbonylamino)-2-methyl-propanoic acid is utilized as a key component in various organic synthesis processes. Its unique structure allows it to participate in a range of chemical reactions, enabling the production of diverse organic compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 91613-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,1 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91613-84:
(7*9)+(6*1)+(5*6)+(4*1)+(3*3)+(2*8)+(1*4)=132
132 % 10 = 2
So 91613-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO4/c1-4-12-6(11)8-7(2,3)5(9)10/h4H2,1-3H3,(H,8,11)(H,9,10)
91613-84-2Relevant academic research and scientific papers
Further studies on the synthesis of symmetrical anhydrides and 2,4-disubstituted-5(4H)-oxazolones from N-alkoxycarbonylamino acids using soluble carbodiimide
Paquet, Alenka,Chen, Francis M. F.,Benoiton, N. Leo
, p. 1335 - 1338 (2007/10/02)
Pure symmetrical anhydrides of N-alkoxycarbonyl (ROCO)-valine, for R=ethyl, tert-butyl, trichloroethyl, p-nitrobenzyl, p-methoxybenzyl, and 9-fluorenylmethyl, and N-ethoxycarbonylaminoisobutyric acid have been prepared using 0.5 equivalents of N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride in dichloromethane followed by removal of side-products by washing with aqueous solutions.When an excess of carbodiimide was uused, 2-alkoxy-5(4H)-oxazolone was also generated, except when R=trichloroethyl.High yields of pure 5(4H)-oxazolone were obtained when R=ethyl.The 2-(9-fluorenylmethyloxy)-5(4H)-oxazolone gradually underwent a β-elimination during manipulation or storage.
