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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)-

5-Bromo-6-(trifluoromethyl)pyrimidin-4-ol

Oc1ncnc(c1Br)C(F)(F)F Request for Quotation
Chemical Name: 5-Bromo-6-(trifluoromethyl)pyrimidin-4-ol
CAS Number: 942060-14-2
Product Number: AG005SN8(AGN-PC-0WAHRA)
Synonyms:
MDL No:
Molecular Formula: C5H2BrF3N2O
Molecular Weight: 242.9814

Identification/Properties

Properties
MP:
225-227°
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
242.983g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
241.93g/mol
Monoisotopic Mass:
241.93g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
281
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P271-P280-P261-P271-P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-6-(trifluoromethyl)pyrimidin-4-ol is a versatile compound widely used in chemical synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as an important intermediate in the synthesis of biologically active molecules due to its unique structure and reactivity. With its bromo and trifluoromethyl functional groups, 5-Bromo-6-(trifluoromethyl)pyrimidin-4-ol can participate in a range of chemical reactions such as nucleophilic substitution, aromatic substitution, and cross-coupling reactions. This compound plays a crucial role in the development of new drugs, herbicides, and materials by enabling the creation of complex molecular structures that exhibit desirable properties for various applications in the chemical industry.