Atomfair N-Benzoylcytidine C16H17N3O6 CAS 13089-48-0

N-Benzoylcytidine (CAS No. 13089-48-0) is a high-purity nucleoside derivative with the molecular formula C16H17N3O6, widely used in biochemical and pharmaceutical research. This compound serves as a protected cytidine analog, where the N4 position is benzoylated to enhance stability and reactivity in oligonucleotide synthesis. With a purity of ≥99%, it is ideal for applications in RNA/DNA modification studies, nucleoside chemistry, and as a building block for antiviral or anticancer drug development. The product is supplied as a white to off-white crystalline powder, soluble in DMSO and methanol, and should be stored at -20°C under inert conditions to maintain integrity. Each batch…

Description

N-Benzoylcytidine (CAS No. 13089-48-0) is a high-purity nucleoside derivative with the molecular formula C16H17N3O6, widely used in biochemical and pharmaceutical research. This compound serves as a protected cytidine analog, where the N4 position is benzoylated to enhance stability and reactivity in oligonucleotide synthesis. With a purity of ≥99%, it is ideal for applications in RNA/DNA modification studies, nucleoside chemistry, and as a building block for antiviral or anticancer drug development. The product is supplied as a white to off-white crystalline powder, soluble in DMSO and methanol, and should be stored at -20°C under inert conditions to maintain integrity. Each batch undergoes rigorous QC testing, including HPLC and NMR analysis, to ensure compliance with research-grade standards.

Properties

  • CAS Number: 13089-48-0
  • Complexity: 586
  • IUPAC Name: N-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-2-oxo-pyrimidin-4-yl]benzamide
  • InChI: InChI=1S/C16H17N3O6/c20-8-10-12(21)13(22)15(25-10)19-7-6-11(18-16(19)24)17-14(23)9-4-2-1-3-5-9/h1-7,10,12-13,15,20-22H,8H2,(H,17,18,23,24)/t10-,12-,13-,15-/m1/s1
  • InChI Key: BNXBRFDWSPXODM-BPGGGUHBSA-N
  • Exact Mass: 347.11173527
  • Molecular Formula: C16H17N3O6
  • Molecular Weight: 347.32
  • SMILES: C1=CC=C(C=C1)C(=O)NC2=NC(=O)N(C=C2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O
  • Topological: 132
  • Monoisotopic Mass: 347.11173527
  • Synonyms: N-benzoylcytidine, 13089-48-0, N4-Benzoylcytidine, DTXSID201316254, DTXCID101746117, 603-444-9, Cytidine, N-benzoyl-, MFCD00010572, N4-Benzoyl-L-cytidine, N-[1-[(2R,3R,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamide, N-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]benzamide, N-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)benzamide, 1018812-31-1, n4-benzoyl-cytidine, 4-n-benzoyl cytidine, N4-Benzoylcytidine, 99%, SCHEMBL565904, N4-Benzoylcytidine;N-(1-(3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)benzamide, AKOS015839054, AKOS015895282, CS-15645, F12710

N-Benzoylcytidine is primarily used in oligonucleotide synthesis as a protected cytidine monomer for solid-phase RNA/DNA assembly. It is also employed in medicinal chemistry for designing nucleoside-based prodrugs targeting viral or tumor cell replication. Researchers utilize this compound in structural biology to study RNA modifications and their functional implications.

Safety and Hazards

GHS Hazard Statements

  • Not Classified
  • Reported as not meeting GHS hazard criteria by 6 of 6 companies. For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

  • Not Classified

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.

Disclaimer

Intended Use & Restrictions

This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.

  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
  • Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).

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