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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)-

4-chloro-5-methyl-6-(2-methylpyridin-3-yl)oxypyrimidine

Cc1ncccc1Oc1ncnc(c1C)Cl Request for Quotation
Chemical Name: 4-chloro-5-methyl-6-(2-methylpyridin-3-yl)oxypyrimidine
CAS Number: 930093-72-4
Product Number: AG00H2QU(AGN-PC-09TPYY)
Synonyms:
MDL No:
Molecular Formula: C11H10ClN3O
Molecular Weight: 235.6696

Identification/Properties

Computed Properties
Molecular Weight:
235.671g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
235.051g/mol
Monoisotopic Mass:
235.051g/mol
Topological Polar Surface Area:
47.9A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
229
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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:
H302-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


4-Chloro-5-methyl-6-((2-methylpyridin-3-yl)oxy)pyrimidine, also known as $name$, serves a crucial role in the field of chemical synthesis. This compound is utilized as a key building block in the development of various organic compounds and pharmaceutical agents. Its unique structure and reactivity make it valuable for the creation of novel molecules with potentially important biological activities. In chemical synthesis, $name$ can be employed as a precursor for the construction of more complex heterocyclic compounds through diverse synthetic routes. The presence of the chloro, methyl, and pyridinyl moieties in its structure allows for versatile manipulation and functionalization, enabling chemists to tailor its properties for specific applications. Additionally, the pyrimidine core confers inherent stability and compatibility with a range of reaction conditions, making $name$ a versatile and valuable tool in the synthesis of diverse chemical entities.