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CAS 32659-31-7

:

4-Amino-1-(5-chloro-5-deoxy-β-D-arabinofuranosyl)-2(1H)-pyrimidinone

Description:
4-Amino-1-(5-chloro-5-deoxy-β-D-arabinofuranosyl)-2(1H)-pyrimidinone, with the CAS number 32659-31-7, is a nucleoside analog that exhibits structural features characteristic of both pyrimidine and sugar moieties. This compound contains an amino group at the 4-position of the pyrimidine ring, which contributes to its biological activity. The presence of a 5-chloro-5-deoxy-β-D-arabinofuranosyl group enhances its potential as an antiviral or anticancer agent, as it can interfere with nucleic acid synthesis. The compound is typically characterized by its solubility in polar solvents, and its stability can be influenced by pH and temperature. Its biological properties are of particular interest in medicinal chemistry, where it may act as an inhibitor of viral replication or as a chemotherapeutic agent. Overall, this compound represents a significant area of research due to its potential therapeutic applications and the unique combination of its structural components.
Formula:C9H12ClN3O4
InChI:InChI=1S/C9H12ClN3O4/c10-3-4-6(14)7(15)8(17-4)13-2-1-5(11)12-9(13)16/h1-2,4,6-8,14-15H,3H2,(H2,11,12,16)/t4-,6-,7+,8-/m1/s1
InChI key:InChIKey=BPGIZMWGUQVFSE-CCXZUQQUSA-N
SMILES:O[C@@H]1[C@@H](O[C@H](CCl)[C@H]1O)N2C(=O)N=C(N)C=C2
Synonyms:
  • 2(1H)-Pyrimidinone, 4-amino-1-(5-chloro-5-deoxy-.beta.-D-arabinofuranosyl)-
  • 2(1H)-Pyrimidinone, 4-amino-1-(5-chloro-5-deoxy-β-<span class="text-smallcaps">D</span>-arabinofuranosyl)-
  • 2′-Chloro-2′-deoxy-1-β-<span class="text-smallcaps">D</span>-arabinofuranosylcytosine
  • 4-Amino-1-(5-chloro-5-deoxy-β-<span class="text-smallcaps">D</span>-arabinofuranosyl)-2(1H)-pyrimidinone
  • 5′-Chloro-5′-deoxyarabinosylcytosine
  • 5′-Chloroarabinosylcytosine
  • NSC 318799
  • 4-Amino-1-(5-chloro-5-deoxy-β-D-arabinofuranosyl)-2(1H)-pyrimidinone
  • 2′-Chloro-2′-deoxy-1-β-D-arabinofuranosylcytosine
  • 2(1H)-Pyrimidinone, 4-amino-1-(5-chloro-5-deoxy-β-D-arabinofuranosyl)-
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