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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, 4-chloro-5-(phenylmethoxy)-

Clc1ncncc1OCc1ccccc1 Request for Quotation
Chemical Name: Pyrimidine, 4-chloro-5-(phenylmethoxy)-
CAS Number: 91063-23-9
Product Number: AG006F0F(AGN-PC-00N9U2)
Synonyms:
MDL No:
Molecular Formula: C11H9ClN2O
Molecular Weight: 220.6550

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
220.656g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
220.04g/mol
Monoisotopic Mass:
220.04g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
185
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


5-(Benzyloxy)-4-chloropyrimidine is a versatile building block commonly used in chemical synthesis for the creation of various organic compounds. This compound plays a crucial role in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a key intermediate in the synthesis of biologically active molecules and heterocyclic compounds due to its unique structural properties.One of the main applications of 5-(Benzyloxy)-4-chloropyrimidine is in the formation of complex molecules through substitution reactions. By selectively modifying the benzyl and chloro substituents on the pyrimidine ring, chemists can access a wide range of structurally diverse compounds with specific properties and functions. This compound also acts as a valuable starting material for the construction of more intricate molecular scaffolds, facilitating the development of new materials and compounds with potential biological or industrial applications.Overall, the strategic use of 5-(Benzyloxy)-4-chloropyrimidine in chemical synthesis enables researchers to efficiently and effectively access novel compounds that can potentially impact various fields, including drug discovery, materials science, and agriculture.