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Oligonucleotide Synthesis, RNA Raw Materials & Modification

7-Deaza-2'-deoxyguanosine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

N.º de productoCH64046N.º CAS86392-75-8Pureza>=98.0%
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Resumen del producto

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Familia de productos
Oligonucleotide Synthesis, RNA Raw Materials & Modification
FM
C11H14N4O4
PM
266.25
Pureza
>=98.0%

7-Deaza-2'-deoxyguanosine (c7dG) is 2'-deoxyguanosine in which the purine N7 nitrogen is replaced by carbon, giving a pyrrolo[2,3-d]pyrimidine base. CH64046 is identified by CAS 86392-75-8, molecular formula C11H14N4O4, molecular weight 266.25, and PubChem CID 135411006.

The cited oligonucleotide literature discusses 7-deaza-dG analogs in base-pairing, duplex-stability, and sequencing band-compression studies where the purine N7 position is being evaluated.

Sinónimos

7-Deaza-2'-deoxyguanosine; c7dG; 7-deaza-dG

Identidad y especificaciones

Catalog No.CH64046
CAS No.86392-75-8
Molecular FormulaC11H14N4O4
Molecular Weight266.25
PubChem CID135411006
InChIKeyPFCLMNDDPTZJHQ-XLPZGREQSA-N
Purity>=98.0%

Condiciones de almacenamiento

2-8 C; keep dark and dry

Atributos técnicos

Nucleobase analog
7-Deazaguanine
Sugar
2'-Deoxyribose
Base modification
7-Deaza (N7 replaced by carbon)
Research role
Modified-oligonucleotide building-block reference
Packaging
100 mg; 250 mg; 1 g; 5 g; Custom packaging on request
Physical form
White to off-white powder

Contexto de aplicación

  • 7-Deazapurine oligonucleotide research: CH64046 is relevant to base-pairing, duplex-stability, and sequencing band-compression studies involving the N7→C base modification.
  • N7-position interaction studies: the 7-deaza base supports comparison of DNA systems where Hoogsteen contacts or metal-binding behavior at the purine N7 position is being evaluated.
  • Base-analog reference: CH64046 provides the 7-deaza-2'-deoxyguanosine identity for nucleoside chemistry research.

Recursos técnicos relacionados

Fuentes públicas

Preguntas frecuentes

What is different about 7-deaza-2'-deoxyguanosine?

The purine N7 nitrogen is replaced by carbon, giving a 7-deazapurine base. This allows comparison of systems where the purine N7 position is relevant to Hoogsteen pairing, metal binding, or sequencing band compression.

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