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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)-

Cytidine, cyclic 2',3'-(hydrogen phosphate), monosodium salt

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Chemical Name: Cytidine, cyclic 2',3'-(hydrogen phosphate), monosodium salt
CAS Number: 15718-51-1
Product Number: AG003P7C(AGN-PC-0Q79F2)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
>209°C (dec.)
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
327.165g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
327.023g/mol
Monoisotopic Mass:
327.023g/mol
Topological Polar Surface Area:
147A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
556
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of Cycliccytidylicacidsodiumsalt (CCAS) in chemical synthesis is versatile and significant. CCAS is commonly employed as a catalyst or reagent in organic chemistry reactions due to its ability to facilitate various transformations with high efficiency and selectivity. In particular, CCAS has found widespread use in the synthesis of nucleoside analogs, which are important compounds in pharmaceutical development for their antiviral and anticancer properties. Additionally, CCAS is utilized in the preparation of modified nucleic acids for research purposes, allowing for the exploration of structure-activity relationships and the development of novel therapeutics. Its versatility and effectiveness make CCAS a valuable tool in the toolbox of synthetic chemists seeking to access complex molecular structures efficiently and economically.