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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)-

5'-Cytidylic acid, disodium salt

O[C@@H]1[C@H](O)[C@H](O[C@H]1n1ccc(nc1=O)N)COP(=O)([O-])[O-].[Na+].[Na+] Request for Quotation
Chemical Name: 5'-Cytidylic acid, disodium salt
CAS Number: 6757-06-8
Product Number: AG003P7E(AGN-PC-0TOWXZ)
Synonyms:
MDL No:
Molecular Formula: C9H12N3Na2O8P
Molecular Weight: 367.1602

Identification/Properties

Properties
MP:
300 °C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
8 ° (C=2, H2O)
Computed Properties
Molecular Weight:
367.161g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
3
Exact Mass:
367.016g/mol
Monoisotopic Mass:
367.016g/mol
Topological Polar Surface Area:
181A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
520
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cytidine 5'-monophosphate disodium salt, also known as CMP-Na2, serves as a vital building block in chemical synthesis processes. This compound is commonly utilized in the production of nucleic acids, where it acts as a precursor for the incorporation of cytidine into DNA and RNA strands. In addition, CMP-Na2 plays a significant role in the preparation of various nucleotide analogs and prodrugs by facilitating the attachment of cytidine moieties to specific molecules. Its ability to enhance the stability and bioavailability of nucleotide-based compounds makes CMP-Na2 an indispensable component in the development of pharmaceuticals and biotechnological products. Furthermore, CMP-Na2 is a versatile tool in organic chemistry, enabling the synthesis of Cytidine derivatives and other complex molecules with tailored functions for diverse applications.