103026-02-4 Usage
Uses
Used in Pharmaceutical Industry:
2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE is used as a potential drug or pharmaceutical intermediate due to its studied biological activities. Its unique structure and properties make it a candidate for further research and development in the creation of new medications or as a component in existing ones.
Used in Research and Development:
In the field of scientific research, 2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE serves as a subject for exploration into its biological activities and potential applications. Researchers utilize 2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE to study its interactions with biological systems and to understand its mechanisms of action, which can contribute to the advancement of medical and pharmaceutical sciences.
Check Digit Verification of cas no
The CAS Registry Mumber 103026-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103026-02:
(8*1)+(7*0)+(6*3)+(5*0)+(4*2)+(3*6)+(2*0)+(1*2)=54
54 % 10 = 4
So 103026-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O/c1-8-9(2)15(12(14)11(8)6-13)7-10-4-3-5-16-10/h3-5H,7,14H2,1-2H3
103026-02-4Relevant articles and documents
Synthesis and rearrangements of 7H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]-and 7h-pyrrolo[3,2-e][1,2,4]triazolo[4,3-c]pyrimidines
Vorob'ev,Kurbatov,Krasnikov,Mezheritskii,Usova
, p. 1492 - 1497 (2007/10/03)
7H-Pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]pyrimidines were synthesized by the reactions of 2-ethoxymethyleneamino-1H-pyrrole-3-carbonitriles with acid hydrazides and by the reactions of aminoiminopyrimidines (prepared based on the above-mentioned carbonitriles) with acid chlorides.
Synthesis of 7-Unsubstituted 7H-Pyrrolopyrimidines
Pichler, Herbert,Folkers, Gerd,Roth, Hermann J.,Eger, Kurt
, p. 1485 - 1505 (2007/10/02)
The title compounds 4 are obtained by N-7 dealkylation of the 2-furanylmethyl, 2-thiophenylmethyl, or 1-phenylethyl group from 2a-g and 10 a-j with polyphosphoric acid.In contrast to the 2-furanylmethyl group the 2-thiophenylmethyl and 1-phenylethyl group