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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)-

2-Pyrimidinemethanol, 4-methyl-

Cc1ccnc(n1)CO Request for Quotation
Chemical Name: 2-Pyrimidinemethanol, 4-methyl-
CAS Number: 142650-13-3
Product Number: AG007KXY(AGN-PC-07AAGF)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O
Molecular Weight: 124.1405

Identification/Properties

Computed Properties
Molecular Weight:
124.143g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
124.064g/mol
Monoisotopic Mass:
124.064g/mol
Topological Polar Surface Area:
46A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
87.1
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-Methylpyrimidin-2-yl)methanol, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various valuable compounds.One of the primary applications of (4-Methylpyrimidin-2-yl)methanol is as a building block in the synthesis of pharmaceutical drugs. Its unique structure allows for the modification of functional groups, enabling the creation of novel drug candidates with improved potency and selectivity. Additionally, (4-Methylpyrimidin-2-yl)methanol serves as a precursor in the synthesis of heterocyclic compounds, which are essential in drug discovery and development.Furthermore, this compound is utilized in the preparation of agrochemicals, such as pesticides and herbicides. By incorporating (4-Methylpyrimidin-2-yl)methanol into the synthesis of these agricultural chemicals, researchers can enhance their effectiveness and specificity towards target pests, ultimately improving crop yield and quality.Overall, (4-Methylpyrimidin-2-yl)methanol is a valuable tool in chemical synthesis, enabling the creation of diverse compounds with important applications in both the pharmaceutical and agricultural sectors.