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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)-

4-Pyridinecarboxylicacid, 2-bromo-3,5-dichloro-

OC(=O)c1c(Cl)cnc(c1Cl)Br Request for Quotation
Chemical Name: 4-Pyridinecarboxylicacid, 2-bromo-3,5-dichloro-
CAS Number: 343781-56-6
Product Number: AG00I6SN(AGN-PC-0KKOV0)
Synonyms:
MDL No:
Molecular Formula: C6H2BrCl2NO2
Molecular Weight: 270.8956

Identification/Properties

Computed Properties
Molecular Weight:
270.891g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
268.865g/mol
Monoisotopic Mass:
268.865g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
192
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:
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-Bromo-3,5-dichloroisonicotinic acid is a valuable intermediate in chemical synthesis processes. It serves as a crucial building block in the creation of various pharmaceutical compounds and agrochemicals. This compound is commonly used in the development of novel molecules with potential biological activities. Its unique structure allows for selective modifications and functional group transformations, making it a versatile tool in organic synthesis. Additionally, 2-Bromo-3,5-dichloroisonicotinic acid plays a significant role in the preparation of new materials for research and industrial applications. Its utility in creating complex structures and facilitating key reactions underscores its importance in modern synthetic chemistry.