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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, 5-methyl-

OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cc(C)c(nc1=O)N Request for Quotation
Chemical Name: Cytidine, 5-methyl-
CAS Number: 2140-61-6
Product Number: AG0034AT(AGN-PC-0O7UQ7)
Synonyms:
MDL No:
Molecular Formula: C10H15N3O5
Molecular Weight: 257.2432

Identification/Properties

Properties
MP:
212-215 °C (dec.)(lit.)
BP:
537.5°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Refractive Index:
15 ° (C=2, H2O)
Computed Properties
Molecular Weight:
257.246g/mol
XLogP3:
-2
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
257.101g/mol
Monoisotopic Mass:
257.101g/mol
Topological Polar Surface Area:
129A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
422
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methylcytidine is a key compound utilized in chemical synthesis for its diverse applications across various industries. As a modified nucleoside derivative, 5-Methylcytidine plays a crucial role in the development of novel pharmaceuticals, agrochemicals, and materials science. This compound is particularly valued for its ability to modulate biological processes, making it a valuable tool in drug discovery and development. In synthetic chemistry, 5-Methylcytidine serves as a versatile building block for the construction of complex molecules, enabling the creation of structurally diverse compounds with tailored properties. Its unique molecular structure and reactivity open up a wide range of possibilities for designing new molecules with enhanced functionalities and improved performance. Whether in the pharmaceutical industry for drug development or in materials science for advanced materials synthesis, 5-Methylcytidine stands out as a valuable resource for innovation and progress.