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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)-

5-bromo-2-(chloromethyl)pyridine hydrochloride

ClCc1ccc(cn1)Br.Cl Request for Quotation
Chemical Name: 5-bromo-2-(chloromethyl)pyridine hydrochloride
CAS Number: 936342-91-5
Product Number: AG0036WM(AGN-PC-09TA21)
Synonyms:
MDL No:
Molecular Formula: C6H6BrCl2N
Molecular Weight: 242.9285

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
242.925g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
240.906g/mol
Monoisotopic Mass:
240.906g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.1
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-2-(chloromethyl)pyridine hydrochloride is a versatile compound that finds extensive application in chemical synthesis. This compound is a valuable building block in organic chemistry due to its unique structure and reactivity. In chemical synthesis, 5-Bromo-2-(chloromethyl)pyridine hydrochloride is commonly used as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its chloromethyl functional group serves as a versatile handle for further derivatization, allowing for the introduction of different substituents and structural modifications.Additionally, this compound is often employed in cross-coupling reactions, such as Suzuki-Miyaura coupling and Negishi coupling, to form carbon-carbon bonds. The presence of both bromine and chlorine atoms in the molecule enables selective transformations, making it a valuable tool in the synthesis of complex organic molecules.Overall, 5-Bromo-2-(chloromethyl)pyridine hydrochloride plays a crucial role in the development of novel chemical entities and the advancement of synthetic methodologies in organic chemistry.