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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-chloro-2-(2-methylpropoxy)pyridin-3-yl]boronic acid

CC(COc1ncc(cc1B(O)O)Cl)C Request for Quotation
Chemical Name: [5-chloro-2-(2-methylpropoxy)pyridin-3-yl]boronic acid
CAS Number: 1217501-42-2
Product Number: AG0015T8(AGN-PC-09PYY8)
Synonyms:
MDL No:
Molecular Formula: C9H13BClNO3
Molecular Weight: 229.4684

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
229.467g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
229.068g/mol
Monoisotopic Mass:
229.068g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
194
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(5-Chloro-2-isobutoxypyridin-3-yl)boronic acid is a versatile compound that plays a crucial role in chemical synthesis. Its high reactivity and compatibility make it an indispensable tool in various synthetic procedures, particularly in the field of organic chemistry.One of the primary applications of (5-Chloro-2-isobutoxypyridin-3-yl)boronic acid is as a boronic acid building block in Suzuki-Miyaura cross-coupling reactions. This reaction is widely used in the synthesis of complex organic molecules and pharmaceutical intermediates. By serving as a coupling partner, (5-Chloro-2-isobutoxypyridin-3-yl)boronic acid facilitates the formation of carbon-carbon bonds, allowing for the creation of new and diverse chemical structures.Additionally, (5-Chloro-2-isobutoxypyridin-3-yl)boronic acid can be employed in the construction of heterocyclic compounds. Its ability to participate in various functional group transformations and selective reactions enables chemists to access a wide range of heterocycles with tailored properties and functionalities.Moreover, this compound can be utilized as a key intermediate in the synthesis of agrochemicals, pharmaceuticals, and materials. Its unique pyridine core and boronic acid functionality offer strategic advantages in the design and optimization of bioactive molecules, making it a valuable building block in drug discovery and development efforts.In conclusion, (5-Chloro-2-isobutoxypyridin-3-yl)boronic acid serves as a valuable reagent in chemical synthesis, enabling the construction of complex molecules, heterocycles, and functional materials. Its versatility and utility make it an essential tool for synthetic chemists striving to expand the frontiers of organic chemistry.