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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-Chloro-4-methyl-6-(2-propen-1-yloxy)pyrimidine

C=CCOc1cc(C)nc(n1)Cl Request for Quotation
Chemical Name: 2-Chloro-4-methyl-6-(2-propen-1-yloxy)pyrimidine
CAS Number: 1250367-45-3
Product Number: AG000N00(AGN-PC-0WAMDT)
Synonyms:
MDL No:
Molecular Formula: C8H9ClN2O
Molecular Weight: 184.6229

Identification/Properties

Computed Properties
Molecular Weight:
184.623g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
184.04g/mol
Monoisotopic Mass:
184.04g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
154
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


2-Chloro-4-methyl-6-(2-propen-1-yloxy)pyrimidine, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound is commonly employed as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules. By serving as a crucial starting material, 2-Chloro-4-methyl-6-(2-propen-1-yloxy)pyrimidine enables the creation of structurally diverse compounds with diverse applications in the fields of medicine, agriculture, and material science.