CAS 115389-03-2

pheac-deoxyguanosine approx. 80%

Description:

Pheac-deoxyguanosine, with the CAS number 115389-03-2, is a modified nucleoside that incorporates a phenylacetyl group into the deoxyguanosine structure. This modification can influence its biochemical properties, such as solubility, stability, and interaction with nucleic acids. Typically, nucleosides like deoxyguanosine are essential components of DNA, playing critical roles in genetic information storage and transfer. The presence of the phenylacetyl group may enhance its ability to participate in various biochemical reactions or improve its pharmacological properties, making it of interest in medicinal chemistry and biochemistry. The approximate purity of 80% suggests that the substance may contain impurities or by-products, which is common in synthetic processes. Characterization techniques such as NMR spectroscopy, mass spectrometry, and HPLC are often employed to confirm the identity and purity of such compounds. Overall, pheac-deoxyguanosine represents a valuable tool in research and potential therapeutic applications, particularly in the fields of molecular biology and drug development.

Formula: C₁₈H₁₉N₅O₆

InChI: InChI=1/C18H19N5O6/c24-7-12-11(25)6-14(29-12)23-9-19-15-16(23)21-18(22-17(15)27)20-13(26)8-28-10-4-2-1-3-5-10/h1-5,9,11-12,14,24-25H,6-8H2,(H2,20,21,22,26,27)/t11-,12+,14+/m0/s1

Synonyms:

• 2-N-Phenylacetylguanoaine
• 2-amino-9-[2-deoxy-5-O-(phenoxyacetyl)pentofuranosyl]-3,9-dihydro-6H-purin-6-one
• 2'-deoxy-N-(phenoxyacetyl)guanosine

2''-Deoxy-N2-phenoxyacetylguanosine

CAS: 115389-03-2

Ref: 7W-GN0314

2'-Deoxy-N2-phenoxyacetylguanosine

CAS: 115389-03-2

2'-deoxy-N2-phenoxyacetylguanosine is a synthetic nucleoside that is used as a substrate in experiments to study the properties of guanine. The compound can be synthesized by the reaction of 2'-deoxy-N2-phenoxyacetaldehyde with guanine. The synthesis starts with the condensation of 2'-deoxyribose and N2-phenoxyacetaldehyde, followed by the oxidation of the resulting anhydride to give aldehyde, which reacts with guanine to form a Schiff base. This then undergoes hydrolysis to yield 2'-deoxy-N2-phenoxyacetylguanosine.

Formula: C₁₈H₁₉N₅O₆

Purity: Min. 95%

Molecular weight: 401.38 g/mol

Ref: 3D-ND08049