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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)-

Pyrimidine, 4,6-dimethyl-2-(methylsulfonyl)-

Cc1cc(C)nc(n1)S(=O)(=O)C Request for Quotation
Chemical Name: Pyrimidine, 4,6-dimethyl-2-(methylsulfonyl)-
CAS Number: 35144-22-0
Product Number: AG007FL8(AGN-PC-0KKUO0)
Synonyms:
MDL No: MFCD03788286
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.2315

Identification/Properties

Computed Properties
Molecular Weight:
186.229g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
186.046g/mol
Monoisotopic Mass:
186.046g/mol
Topological Polar Surface Area:
68.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
235
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:
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


4,6-Dimethyl-2-methylsulfonylpyrimidine is a versatile compound widely utilized in chemical synthesis as a potent building block. Its unique structure enables it to participate in various reactions, making it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, 4,6-Dimethyl-2-methylsulfonylpyrimidine serves as a key reagent for the synthesis of complex molecules due to its ability to introduce functional groups and promote desired transformations. Its utility in cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations has established it as a vital component in the toolkit of synthetic chemists seeking efficient routes to target molecules. Additionally, the sulfonyl moiety in 4,6-Dimethyl-2-methylsulfonylpyrimidine imparts stability and enhances the reactivity of the compound, expanding its applicability in diverse chemical transformations.