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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)-

Uridine, 2'-O-(2-methoxyethyl)-5-methyl-

COCCO[C@@H]1[C@H](O)[C@H](O[C@H]1n1cc(C)c(=O)[nH]c1=O)CO Request for Quotation
Chemical Name: Uridine, 2'-O-(2-methoxyethyl)-5-methyl-
CAS Number: 163759-49-7
Product Number: AG00ANEX(AGN-PC-0O4OEI)
Synonyms:
MDL No:
Molecular Formula: C13H20N2O7
Molecular Weight: 316.3071

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
316.31g/mol
XLogP3:
-1.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
6
Exact Mass:
316.127g/mol
Monoisotopic Mass:
316.127g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
467
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2'-O-(2-Methoxyethyl)-5-methyluridine, also known as $name$, is a versatile nucleoside derivative that finds extensive application in chemical synthesis. This compound serves as a valuable building block in the synthesis of modified nucleotides and oligonucleotides with enhanced properties and functions.In chemical synthesis, 2'-O-(2-Methoxyethyl)-5-methyluridine is commonly utilized in the development of nucleic acid analogs for various research purposes. Its unique structural characteristics make it an ideal candidate for introducing specific modifications into nucleic acid sequences, such as mRNA, siRNA, and antisense oligonucleotides.Furthermore, the presence of the 2'-O-(2-Methoxyethyl) group in this compound provides stability and protection to the nucleoside, making it more resistant to degradation by nucleases. This feature is particularly advantageous in the design of nucleic acid-based therapeutics and diagnostics, where stability and specificity are crucial for their effectiveness.Overall, the application of 2'-O-(2-Methoxyethyl)-5-methyluridine in chemical synthesis enables researchers to tailor nucleic acid structures with precision, opening up new possibilities for the development of advanced biomaterials and molecular tools.