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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)-

2,4-dibromo-3-chloropyridine

Clc1c(Br)ccnc1Br Request for Quotation
Chemical Name: 2,4-dibromo-3-chloropyridine
CAS Number: 861024-77-3
Product Number: AG00GULR(AGN-PC-0JWHTR)
Synonyms:
MDL No:
Molecular Formula: C5H2Br2ClN
Molecular Weight: 271.33708

Identification/Properties

Computed Properties
Molecular Weight:
271.336g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
270.822g/mol
Monoisotopic Mass:
268.824g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
101
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:
Danger
UN#:
2810
Hazard Statements:
H301-H311-H331
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dibromo-3-chloropyridine is a versatile building block extensively utilized in organic synthesis. This compound plays a crucial role in various chemical reactions and serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials with advanced properties.Chemists often employ 2,4-Dibromo-3-chloropyridine in the synthesis of complex organic molecules due to its unique reactivity and structural features. It serves as a valuable substrate for introducing functional groups such as alkyl, aryl, and heterocyclic moieties through substitution or coupling reactions.In pharmaceutical synthesis, 2,4-Dibromo-3-chloropyridine is commonly used as a precursor for creating novel drug candidates with potential therapeutic properties. Its structural scaffold enables chemical modification to optimize biological activity and enhance pharmacokinetic profiles.Furthermore, in the field of agrochemicals, this compound is instrumental in developing crop protection agents and herbicides that target specific pests or unwanted plant species. By functionalizing 2,4-Dibromo-3-chloropyridine, chemists can tailor the molecular structure to improve efficacy and environmental compatibility.Additionally, in materials science, the structural diversity of 2,4-Dibromo-3-chloropyridine enables its incorporation into polymers, liquid crystals, and other advanced materials. Through controlled synthetic pathways, researchers can tune the physical and chemical properties of these materials for various industrial applications.Overall, the strategic utility of 2,4-Dibromo-3-chloropyridine in chemical synthesis underscores its significance as a valuable building block for creating diverse compounds with diverse functions and applications.