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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)-

Guanosine 5'-(trihydrogen diphosphate), P'-anhydride withphosphorothioic acid, tetralithium salt

O[C@@H]1[C@@H](COP(=O)(OP(=O)(OP(=S)([O-])[O-])[O-])[O-])O[C@H]([C@@H]1O)n1cnc2c1nc(N)[nH]c2=O.[Li+].[Li+].[Li+].[Li+] Request for Quotation
Chemical Name: Guanosine 5'-(trihydrogen diphosphate), P'-anhydride withphosphorothioic acid, tetralithium salt
CAS Number: 94825-44-2
Product Number: AG005V2I(AGN-PC-0W4GZ7)
Synonyms:
MDL No: MFCD00135151
Molecular Formula: C10H12Li4N5O13P3S
Molecular Weight: 562.9783

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;Inert atmosphere;
Computed Properties
Molecular Weight:
562.969g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
16
Rotatable Bond Count:
8
Exact Mass:
563.001g/mol
Monoisotopic Mass:
563.001g/mol
Topological Polar Surface Area:
321A^2
Heavy Atom Count:
36
Formal Charge:
0
Complexity:
916
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:
5
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Guanosine 5′-(trihydrogen diphosphate), P′-anhydride with phosphorothioic acid, lithium salt (1:4) is a versatile compound widely used in chemical synthesis. Its unique composition allows it to serve as a crucial building block in the production of nucleic acids, such as RNA and DNA, making it an essential component in genetic engineering and pharmaceutical research. Additionally, this compound is instrumental in the development of modified oligonucleotides and analogs for various biotechnological applications. Its ability to participate in selective chemical reactions makes it highly valuable in the synthesis of specialized nucleotide derivatives for use in molecular biology and medicinal chemistry.