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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)-

Boronic acid, B-(5,6-dichloro-3-pyridinyl)-

OB(c1cnc(c(c1)Cl)Cl)O Request for Quotation
Chemical Name: Boronic acid, B-(5,6-dichloro-3-pyridinyl)-
CAS Number: 1072944-15-0
Product Number: AG008S6Z(AGN-PC-07HAWH)
Synonyms:
MDL No:
Molecular Formula: C5H4BCl2NO2
Molecular Weight: 191.8078

Identification/Properties

Computed Properties
Molecular Weight:
191.802g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
190.971g/mol
Monoisotopic Mass:
190.971g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
138
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dichloropyridine-5-boronic acid is a versatile compound commonly used in chemical synthesis as a key building block. With its unique structure, this boronic acid derivative is highly valued for its ability to participate in various organic reactions, particularly in the field of medicinal and material chemistry.One of the primary applications of 2,3-Dichloropyridine-5-boronic acid is in Suzuki-Miyaura cross-coupling reactions, where it serves as a crucial component in forming carbon-carbon bonds. This reaction allows for the creation of complex molecular structures by joining different organic fragments together efficiently and selectively.Additionally, this compound is utilized in the synthesis of pharmaceutical intermediates, agrochemicals, and functional materials. Its compatibility with a wide range of functional groups and its stability under reaction conditions make it a valuable tool for organic chemists seeking to design and construct diverse compounds.Overall, 2,3-Dichloropyridine-5-boronic acid plays a key role in advancing chemical synthesis processes, enabling the creation of novel molecules with potential applications in various scientific fields.