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1418287-34-9

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  • 1-TERT-BUTYL 2-METHYL 4-CHLORO-1H-PYRROLO[3,2-C]PYRIDINE-1,2-DICARBOXYLATE

    Cas No: 1418287-34-9

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1418287-34-9 Usage

Pyrrolopyridine derivative

The compound is derived from a pyrrolopyridine structure, which is a five-membered ring containing both pyrrole and pyridine moieties.

Common use as intermediate

The compound is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, meaning it is a key component in the production of other chemical compounds.

Antimicrobial and antiviral properties

1-tert-butyl 2-methyl 4-chloro-1H-pyrrolo[3,2-c]pyridine-1,2-dicarboxylate has demonstrated the ability to inhibit the growth of microorganisms and viruses, making it a potential candidate for treating infections.

Potential use in treating diseases

The compound has been studied for its potential applications in treating various diseases, including cancer and infectious diseases, due to its biological activities.

Versatile compound for research and development

The chemical structure and properties of 1-tert-butyl 2-methyl 4-chloro-1H-pyrrolo[3,2-c]pyridine-1,2-dicarboxylate make it a valuable compound for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1418287-34-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,8,2,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1418287-34:
(9*1)+(8*4)+(7*1)+(6*8)+(5*2)+(4*8)+(3*7)+(2*3)+(1*4)=169
169 % 10 = 9
So 1418287-34-9 is a valid CAS Registry Number.

1418287-34-9Relevant articles and documents

Mild one-pot Horner-Wadsworth-Emmons olefination and intramolecular N-arylation for the syntheses of indoles, all regio-isomeric azaindoles, and thienopyrroles

Choi, Ji Hye,Lim, Hwan Jung

, p. 5131 - 5138 (2015)

The syntheses of various N-protected aromatic-ring fused pyrrole-2-carboxylate derivatives have been accomplished using mild one-pot Horner-Wadsworth-Emmons olefination and Cu-catalyzed intramolecular N-arylation reactions. The optimized mild one-pot reac

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