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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-6-propyl-

CCCc1cc(Cl)nc(n1)Cl Request for Quotation
Chemical Name: Pyrimidine, 2,4-dichloro-6-propyl-
CAS Number: 89938-07-8
Product Number: AG006NXZ(AGN-PC-07H7Y5)
Synonyms:
MDL No:
Molecular Formula: C7H8Cl2N2
Molecular Weight: 191.0578

Identification/Properties

Properties
BP:
261.8 °C at 760 mmHg
Computed Properties
Molecular Weight:
191.055g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
190.006g/mol
Monoisotopic Mass:
190.006g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
121
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


The compound 2,4-Dichloro-6-propylpyrimidine is widely utilized in chemical synthesis as a versatile building block in the production of various pharmaceuticals and agrochemicals. With its unique structure and reactivity, this compound serves as a key intermediate in the synthesis of complex organic molecules. In particular, 2,4-Dichloro-6-propylpyrimidine plays a crucial role in the development of novel drugs and crop protection agents due to its ability to undergo selective functionalization reactions. By incorporating this compound into synthetic routes, chemists can access a diverse array of derivatives with improved biological activities and targeted properties.