Atomfair 6-Chloro-7-iodo-7-deazapurine C6H3ClIN3

Description 6-Chloro-7-iodo-7-deazapurine (CAS No. 123148-78-7) is a high-purity heterocyclic compound with the molecular formula C6H3ClIN3and IUPAC name 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine . This specialized chemical is a halogenated derivative of 7-deazapurine, featuring both chloro and iodo functional groups, making it a versatile intermediate for nucleoside synthesis and medicinal chemistry applications. Its unique structure allows for selective modifications, enabling researchers to develop novel pharmaceuticals, agrochemicals, or biochemical probes. Our product is rigorously tested for purity and stability, ensuring reliable performance in demanding laboratory environments. Available in various quantities, this compound is ideal for researchers seeking a high-quality building block for complex organic syntheses.

Description

6-Chloro-7-iodo-7-deazapurine (CAS No. 123148-78-7) is a high-purity heterocyclic compound with the molecular formula C₆H₃ClIN₃ and IUPAC name 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine. This specialized chemical is a halogenated derivative of 7-deazapurine, featuring both chloro and iodo functional groups, making it a versatile intermediate for nucleoside synthesis and medicinal chemistry applications. Its unique structure allows for selective modifications, enabling researchers to develop novel pharmaceuticals, agrochemicals, or biochemical probes. Our product is rigorously tested for purity and stability, ensuring reliable performance in demanding laboratory environments. Available in various quantities, this compound is ideal for researchers seeking a high-quality building block for complex organic syntheses.

CAS No: 123148-78-7
Molecular Formula: C6H3ClIN3
Molecular Weight: 279.46
Exact Mass: 278.90602
Monoisotopic Mass: 278.90602
IUPAC Name: 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine
SMILES: C1=C(C2=C(N1)N=CN=C2Cl)I
Synonyms: 6-Chloro-7-iodo-7-deazapurine, 626-377-7, 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine, 123148-78-7, 4-Chloro-5-iodo-7H-pyrrol[2,3-d]pyrimidine

Application

6-Chloro-7-iodo-7-deazapurine serves as a key intermediate in the synthesis of modified nucleosides and nucleotides, particularly in antiviral and anticancer drug development. Its reactive halogen groups enable efficient cross-coupling reactions, such as Suzuki or Sonogashira couplings, for creating diverse purine analogs. Researchers also utilize this compound in the study of enzyme inhibition and as a precursor for fluorescent or radiolabeled probes in biochemical assays.

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