7026-48-4 Usage
Molecular structure
1H-Imidazole-4-carboxamide, 1-(phenylmethyl)-5-[(phenylmethyl)amino]is a chemical compound that consists of an imidazole ring with a carboxamide group, a phenylmethyl group attached to the first position, and a phenylmethylamino group attached to the fifth position.
Classification
It belongs to the imidazole class of compounds.
Derivative
It is a derivative of imidazole-4-carboxamide with a 1-(phenylmethyl) group and a 5-[(phenylmethyl)amino] substituent.
Pharmaceutical industry use
It is commonly used in the pharmaceutical industry due to its potential pharmacological properties.
Enzyme or receptor inhibition
It can act as an inhibitor for certain enzymes or receptors, making it a potential candidate for drug development.
Precursor or intermediate in organic synthesis
It can also be used as a precursor or intermediate in the synthesis of other organic compounds.
Diverse applications
It has diverse applications in the field of medicine and organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 7026-48-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7026-48:
(6*7)+(5*0)+(4*2)+(3*6)+(2*4)+(1*8)=84
84 % 10 = 4
So 7026-48-4 is a valid CAS Registry Number.
7026-48-4Relevant academic research and scientific papers
SYNTHESIS OF N,N,3,9-TETRALAKYLADENINIUM HALIDES BY ALKYLATIONS OF N,N,3- AND N,N,9-TRIALKYLADENINES
Itaya, Taisuke,Ogawa, Kazuo,Matsumoto, Hiroo,Watanabe, Tomoko
, p. 2522 - 2527 (2007/10/02)
The reactions of N,N,9-trialkyladenines (II) with alkyl halides in N,N-dimethylacetamide gave N,N,3,9-tetraalkyladeninium halides (!V) in good yields.N,N,3-trialkyladenines (III) underwent the alkylation more smoothly to provide an alternative synthesis o
