129179-30-2 Usage
General Description
2-(Chloromethyl)-3-nitroimidazo[1,2-a]pyridine is a chemical compound with the molecular formula C7H5ClN4O2. It is a derivative of the imidazole ring system and is known for its potential use as an antiprotozoal agent. 2-(CHLOROMETHYL)-3-NITROIMIDAZO[1,2-A]PYRIDINE is notable for its nitro group and chloromethyl functional group, both of which are important for its biological activity. The nitro group is often associated with potential anti-infective properties, while the chloromethyl group can serve as a reactive site for further chemical modification. The specific properties and potential applications of 2-(Chloromethyl)-3-nitroimidazo[1,2-a]pyridine make it a subject of interest in medicinal and synthetic chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 129179-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,7 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129179-30:
(8*1)+(7*2)+(6*9)+(5*1)+(4*7)+(3*9)+(2*3)+(1*0)=142
142 % 10 = 2
So 129179-30-2 is a valid CAS Registry Number.
129179-30-2Relevant articles and documents
Design, Synthesis, Anti-Cancer Activity, and in silico Studies of Novel Imidazo[1,2-a]pyridine Derivatives
Bodige, S.,Chandra, J. N. Narendra Sharath,Endoori, S.,Gulipalli, K. C.,Seelam, N.
, p. 1727 - 1736 (2020)
Abstract: A novel series of imidazo [1,2-a]pyridinederivatives has been designed, synthesized and tested for the anti-proliferativeactivity against three different human cancer cell lines. Most of thesynthesized compounds exhibit anti-proliferative activi
Synthesis by the S(RN)1 reaction of a new series of imidazo[1,2-a]pyridine derivatives with pharmacological potentialities
Vanelle,Madadi,Roubaud,Maldonado,Crozet
, p. 5173 - 5184 (2007/10/02)
The study of S(RN)1 reaction between 2-chloromethyl-3-nitroimidazo[1,2-a] pyridine and 2-nitropropane salts has been extended to various aliphatic, cyclic and heterocyclic nitronate anions. From C-alkylation products, base-promoted nitrous acid elimination afforded new potential pharmacological derivatives with a trisubstituted double bond at the 2 position.
