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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)-

Pyridine, 5-bromo-2-(cyclopropylmethoxy)-

Brc1ccc(nc1)OCC1CC1 Request for Quotation
Chemical Name: Pyridine, 5-bromo-2-(cyclopropylmethoxy)-
CAS Number: 494772-02-0
Product Number: AG003MFZ(AGN-PC-03HN87)
Synonyms:
MDL No:
Molecular Formula: C9H10BrNO
Molecular Weight: 228.0858

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
228.089g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
226.995g/mol
Monoisotopic Mass:
226.995g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
150
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


5-Bromo-2-(cyclopropylmethoxy)pyridine, also known as $name$, is a versatile compound widely used in chemical synthesis. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure, which combines a bromine atom and a cyclopropylmethoxy group on a pyridine ring, imparts distinct reactivity that enables a range of synthetic transformations.One notable application of 5-Bromo-2-(cyclopropylmethoxy)pyridine is in the formation of heterocyclic compounds through cross-coupling reactions. By leveraging the reactivity of the bromine atom, chemists can selectively introduce the cyclopropylmethoxy group onto different aromatic systems, allowing for the efficient construction of diverse chemical scaffolds. This compound's ability to participate in various synthetic pathways makes it a valuable tool for the preparation of complex molecular structures with specific functionalities tailored for various applications in the fields of medicine, agriculture, and materials science.