126866-37-3 Usage
Description
2-AMINO-N-METHYL-N-PHENYL-ACETAMIDE is an organic compound that serves as a key reactant in the development of various chemical and pharmaceutical applications. It is characterized by its unique molecular structure, which includes an amide functional group and a phenyl ring, making it a versatile building block for the synthesis of new compounds.
Uses
Used in Pharmaceutical Industry:
2-AMINO-N-METHYL-N-PHENYL-ACETAMIDE is used as a reactant for the design and synthesis of novel diamide derivatives of glycine. These derivatives have potential applications as antihyperglycemic agents, which can help in the management and treatment of diabetes by regulating blood sugar levels.
In the synthesis process, 2-AMINO-N-METHYL-N-PHENYL-ACETAMIDE acts as a crucial component, contributing to the formation of the desired diamide derivatives. Its reactivity and structural properties enable the creation of new compounds with improved pharmacological properties, such as enhanced efficacy, selectivity, and reduced side effects.
Furthermore, the use of 2-AMINO-N-METHYL-N-PHENYL-ACETAMIDE in the pharmaceutical industry highlights its potential for contributing to the development of innovative therapeutic solutions for various health conditions, particularly those related to metabolic disorders like diabetes.
Check Digit Verification of cas no
The CAS Registry Mumber 126866-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,6 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126866-37:
(8*1)+(7*2)+(6*6)+(5*8)+(4*6)+(3*6)+(2*3)+(1*7)=153
153 % 10 = 3
So 126866-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O/c1-11(9(12)7-10)8-5-3-2-4-6-8/h2-6H,7,10H2,1H3
126866-37-3Relevant articles and documents
Access to newly functionalized imidazole derivatives: Efficient synthesis of novel 5-amino-2-thioimidazoles using propylphosphonic anhydride (T3P)
Lasalle, Manuel,Picon, Sylvain,Boulahjar, Rajaa,Hoguet, Vanessa,Van Obbergen, Jolien,Roussel, Pascal,Deprez, Benoit,Charton, Julie
supporting information, p. 1011 - 1014 (2015/02/19)
We describe here an efficient method to synthesize 5-amino-2-thioimidazole compounds by T3P-mediated cyclization of N-acetamidoisothiourea intermediates. The newly functionalized 5-amino-2-thioimidazole compounds are finally obtained in 5 steps from an amine as starting block.
