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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)-

Cytidine5'-(trihydrogen diphosphate), 2'-deoxy-, trisodium salt, hydrate (9CI)

O[C@H]1C[C@@H](O[C@@H]1COP(=O)(OP(=O)([O-])[O-])[O-])n1ccc(nc1=O)N.[Na+].[Na+].[Na+] Request for Quotation
Chemical Name: Cytidine5'-(trihydrogen diphosphate), 2'-deoxy-, trisodium salt, hydrate (9CI)
CAS Number: 151151-32-5
Product Number: AG00HXUK(AGN-PC-0Q5PGS)
Synonyms:
MDL No:
Molecular Formula: C9H12N3Na3O10P2
Molecular Weight: 453.1225

Identification/Properties

Computed Properties
Molecular Weight:
453.123g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
5
Exact Mass:
452.969g/mol
Monoisotopic Mass:
452.969g/mol
Topological Polar Surface Area:
210A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
640
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
4
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301+H311+H331-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338-P311
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2'-Deoxycytidine-5'-diphosphate trisodium salt is a vital component in chemical synthesis processes due to its significance in nucleotide chemistry. Specifically, this nucleotide derivative serves as a critical building block in the creation of DNA and RNA molecules, playing a key role in the assembly of genetic material. In chemical synthesis, 2'-Deoxycytidine-5'-diphosphate trisodium salt is utilized to facilitate the formation of phosphodiester bonds during the construction of nucleic acid chains. Its incorporation allows for the controlled and precise linking of nucleotide units, enabling the generation of customized DNA or RNA sequences with high accuracy. Furthermore, this compound's unique properties make it an essential tool in the development of pharmaceuticals, bioconjugates, and other biologically active molecules where the accurate replication of nucleic acid sequences is crucial.