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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'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-methyl-N-(2-methyl-1-oxopropyl)-

COc1ccc(cc1)C(c1ccc(cc1)OC)(c1ccccc1)OC[C@H]1O[C@H]([C@@H]([C@@H]1O)OC)n1cnc2c1nc(NC(=O)C(C)C)[nH]c2=O Request for Quotation
Chemical Name: Guanosine,5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-methyl-N-(2-methyl-1-oxopropyl)-
CAS Number: 114745-26-5
Product Number: AG000F4X(AGN-PC-0P6OKK)
Synonyms:
MDL No:
Molecular Formula: C36H39N5O8
Molecular Weight: 669.7236

Identification/Properties

Computed Properties
Molecular Weight:
669.735g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
12
Exact Mass:
669.28g/mol
Monoisotopic Mass:
669.28g/mol
Topological Polar Surface Area:
155A^2
Heavy Atom Count:
49
Formal Charge:
0
Complexity:
1130
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

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Chemical Structure


$name$ is a unique derivative used in chemical synthesis for its versatile applications in the production of oligonucleotides and nucleic acid analogs. Specifically, the 5'-DMT-2'-OMe-ibu-G modification serves as a valuable building block in the creation of custom DNA and RNA sequences with enhanced stability and specific functionalities. By incorporating $name$ into oligonucleotide structures, researchers can tailor the properties of the synthesized molecules for various research, diagnostic, and therapeutic purposes. This modification offers precise control over the structure and behavior of nucleic acids, enabling the design of sophisticated molecular tools for a wide range of biotechnological and biomedical applications.