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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, 2,4-dichloro-5-ethyl-

CCc1cnc(nc1Cl)Cl Request for Quotation
Chemical Name: Pyrimidine, 2,4-dichloro-5-ethyl-
CAS Number: 34171-40-9
Product Number: AG00CIQV(AGN-PC-0MX95L)
Synonyms:
MDL No:
Molecular Formula: C6H6Cl2N2
Molecular Weight: 177.0312

Identification/Properties

Properties
BP:
246°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
177.028g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
175.991g/mol
Monoisotopic Mass:
175.991g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dichloro-5-ethylpyrimidine is a versatile compound extensively utilized in chemical synthesis due to its unique properties and reactivity. In the realm of organic chemistry, this compound serves as a crucial building block for the synthesis of various pharmaceuticals, agrochemicals, and materials.One key application of 2,4-Dichloro-5-ethylpyrimidine is its use as a precursor in the synthesis of novel pyrimidine-based drugs. Through strategic functionalization and manipulation of its chemical structure, researchers can create new drugs with enhanced pharmacological properties and bioactivity. Additionally, its role in medicinal chemistry extends to the development of potential anti-cancer agents, antiviral drugs, and other therapeutic agents.Furthermore, in the field of agrochemicals, 2,4-Dichloro-5-ethylpyrimidine is employed in the synthesis of pesticides and herbicides. By incorporating this compound into the chemical structure of agrochemicals, scientists can design more effective and environmentally friendly crop protection products.Moreover, in material science, 2,4-Dichloro-5-ethylpyrimidine finds application as a building block for the synthesis of specialized polymers and functional materials. Its incorporation into polymer chains imparts specific properties such as enhanced durability, thermal stability, or conductivity, making it a valuable component in the development of advanced materials for various industrial applications.