1. Home
  2. Cytidine, 5-chloro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Cytidine, 5-chloro-

OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cc(Cl)c(nc1=O)N Request for Quotation
Chemical Name: Cytidine, 5-chloro-
CAS Number: 25130-29-4
Product Number: AG002QKG(AGN-PC-0O898N)
Synonyms:
MDL No:
Molecular Formula: C9H12ClN3O5
Molecular Weight: 277.6617

Identification/Properties

Computed Properties
Molecular Weight:
277.661g/mol
XLogP3:
-1.5
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
277.047g/mol
Monoisotopic Mass:
277.047g/mol
Topological Polar Surface Area:
129A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
426
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-Chlorocytidine is a versatile compound widely used in chemical synthesis for its unique properties and applications. This compound plays a crucial role in nucleoside chemistry, where it functions as a key intermediate for the synthesis of various nucleoside analogs and pharmaceuticals. Its specific chemical structure and reactivity make it an essential building block in the creation of new bioactive compounds.In organic chemistry, 5-Chlorocytidine serves as a valuable starting material for the modification of nucleosides, allowing for the introduction of specific functional groups or structural modifications to tailor the properties of the resulting molecules. Its ability to undergo various coupling reactions, such as cross-coupling and substitution reactions, makes it an indispensable tool for chemical synthesis.Moreover, 5-Chlorocytidine is utilized in the development of antiviral and anticancer agents due to its ability to inhibit nucleic acid synthesis, making it a promising candidate for drug discovery and development. Its incorporation into nucleoside analogs has shown potential in targeting viral infections and cancer cells by disrupting their replication processes.Overall, the application of 5-Chlorocytidine in chemical synthesis highlights its significance in creating novel nucleoside derivatives with therapeutic potential, paving the way for the advancement of medicinal chemistry and drug design efforts.