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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, (6-chloro-3-pyridinyl)-

Clc1ccc(cn1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (6-chloro-3-pyridinyl)-
CAS Number: 444120-91-6
Product Number: AG00339M(AGN-PC-0L0VW0)
Synonyms:
MDL No: MFCD03094998
Molecular Formula: C5H5BClNO2
Molecular Weight: 157.3627

Identification/Properties

Properties
MP:
165 °C
BP:
336.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
157.36g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
157.01g/mol
Monoisotopic Mass:
157.01g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
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-Chloropyridine-5-boronic acid is a highly versatile compound widely used in chemical synthesis processes. In the field of organic chemistry, this compound serves as a crucial building block for the construction of complex molecules. Its boronic acid functionality allows for efficient Suzuki-Miyaura cross-coupling reactions with various aryl and heteroaryl halides, enabling the formation of new carbon-carbon bonds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, 2-Chloropyridine-5-boronic acid can be employed in the production of functionalized aromatic compounds, which are valuable intermediates in the preparation of dyes, polymers, and other specialty chemicals. Its compatibility with a range of reaction conditions and its ability to facilitate selective transformations make it a valuable tool for chemists working in diverse research areas.