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Oligonucleotide Synthesis, RNA Raw Materials & Modification

5-TFA-ap-2'-deoxyuridine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

N° produitCH64053N° CAS115899-40-6Pureté98%
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Résumé du produit

Aperçu rapide

Famille de produits
Oligonucleotide Synthesis, RNA Raw Materials & Modification
FM
C14H14F3N3O6
PM
377.27
Pureté
98%

5-TFA-ap-2'-deoxyuridine is 2'-deoxyuridine that carries a 3-(trifluoroacetamido)prop-1-ynyl amino-linker at the C5 position of uracil. CH64053 is identified by CAS 115899-40-6, molecular formula C14H14F3N3O6, molecular weight 377.27, PubChem CID 10894132, and InChIKey HCKMZBZCHQQZRJ-IVZWLZJFSA-N.

The trifluoroacetyl (TFA) group protects a primary amine on the aminopropynyl linker. The cited labeling literature discusses amine-linker nucleosides as motifs for covalent fluorophore attachment in nucleoside and oligonucleotide labeling research.

Synonymes

5-(3-trifluoroacetamidoprop-1-ynyl)-2'-deoxyuridine; 5-TFA-ap-dU

Identité et spécifications

Catalog No.CH64053
CAS No.115899-40-6
Molecular FormulaC14H14F3N3O6
Molecular Weight377.27
PubChem CID10894132
InChIKeyHCKMZBZCHQQZRJ-IVZWLZJFSA-N
Purity98%

Conditions de stockage

Room temperature

Caractéristiques techniques

Nucleobase
Uracil
Sugar
2'-Deoxyribose
C5 linker
3-Aminoprop-1-ynyl
Amine protection
Trifluoroacetyl (TFA)
Packaging
100 mg; 250 mg; 1 g; Custom packaging on request

Contexte d’application

  • Internal-labeling research: CH64053 combines a 2'-deoxyuridine identity with a C5 aminopropynyl linker for oligonucleotide labeling studies.
  • Amine-linker labeling studies: the TFA-protected aminopropynyl group represents a protected amine-linker motif discussed for covalent fluorophore attachment after deprotection.
  • Base-analog reference: CH64053 provides the 5-TFA-ap-2'-deoxyuridine identity for nucleoside chemistry research.

Ressources techniques associées

Sources publiques

Questions fréquentes

What do 'TFA' and 'ap' mean in the name?

'ap' is the aminopropynyl (3-aminoprop-1-ynyl) linker at the C5 position of uracil, and 'TFA' is the trifluoroacetyl group protecting that linker's primary amine.

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