CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

7-Deaza-2'-deoxyadenosine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

製品番号CH64045CAS番号60129-59-1純度>98%
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製品概要

クイックビュー

製品ファミリー
Oligonucleotide Synthesis, RNA Raw Materials & Modification
分子式
C11H14N4O3
分子量
250.25
純度
>98%

7-Deaza-2'-deoxyadenosine, also called 2'-deoxytubercidin (c7dA), is 2'-deoxyadenosine in which the purine N7 nitrogen is replaced by carbon, giving a pyrrolo[2,3-d]pyrimidine base. CH64045 is identified by CAS 60129-59-1, molecular formula C11H14N4O3, molecular weight 250.25, and PubChem CID 3006222.

The cited oligonucleotide literature discusses 7-deaza-dA analogs in base-pairing, metal-mediated base-pair, and duplex-stability studies where the N7 position is being examined. CH64045 provides the 7-deaza-2'-deoxyadenosine identity for related base-analog research.

別名

7-Deaza-2'-deoxyadenosine; 2'-deoxytubercidin; c7dA; 7-deaza-dA

同定情報と仕様

Catalog No.CH64045
CAS No.60129-59-1
Molecular FormulaC11H14N4O3
Molecular Weight250.25
PubChem CID3006222
InChIKeyNIJSNUNKSPLDTO-DJLDLDEBSA-N
Purity>98%

保管条件

2-8 C; keep dark and dry

技術属性

Nucleobase analog
7-Deazaadenine
Sugar
2'-Deoxyribose
Base modification
7-Deaza (N7 replaced by carbon)
Research role
Modified-oligonucleotide building-block reference
Packaging
500 mg; 1 g; 10 g; 25 g; 50 g; 100 g; Custom packaging on request
Physical form
White to off-white powder

用途情報

  • 7-Deazapurine oligonucleotide research: CH64045 is relevant to base-pairing, metal-mediated base-pair, and duplex-stability studies involving the N7→C base modification.
  • N7-position interaction studies: the 7-deaza base helps compare DNA systems where Hoogsteen or metal-binding behavior at the purine N7 position is being evaluated.
  • Base-analog reference: CH64045 provides the 7-deaza-2'-deoxyadenosine identity for nucleoside chemistry research.

関連技術資料

公開情報源

よくある質問

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

The purine N7 nitrogen is replaced by carbon, forming a 7-deazapurine / pyrrolo[2,3-d]pyrimidine base. This removes the N7 site considered in Hoogsteen and metal-binding studies.

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