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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(1H)-Pyrimidinone, 2-(methylthio)-6-(trifluoromethyl)-

CSc1nc(cc(=O)[nH]1)C(F)(F)F Request for Quotation
Chemical Name: 4(1H)-Pyrimidinone, 2-(methylthio)-6-(trifluoromethyl)-
CAS Number: 16097-62-4
Product Number: AG001VJO(AGN-PC-0JOKBW)
Synonyms:
MDL No:
Molecular Formula: C6H5F3N2OS
Molecular Weight: 210.1769

Identification/Properties

Properties
MP:
176-180°C(lit.);
BP:
205.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
210.174g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
210.007g/mol
Monoisotopic Mass:
210.007g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
295
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Methylthio)-6-(trifluoromethyl)pyrimidin-4-ol is a highly versatile compound used in chemical synthesis for its unique properties. This compound serves as an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. It plays a crucial role in the development of novel drugs and compounds due to its capability to act as a building block in organic reactions. Known for its stability and reactivity, 2-(Methylthio)-6-(trifluoromethyl)pyrimidin-4-ol is widely utilized in medicinal chemistry to create bioactive molecules with enhanced pharmacological properties. Additionally, this compound is employed in the synthesis of complex organic compounds with specific functionalities, making it a valuable tool for chemical research and development.