1. Home
  2. [5-(2-hydroxypropan-2-yl)pyridin-3-yl]boronic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-(2-hydroxypropan-2-yl)pyridin-3-yl]boronic acid

OB(c1cncc(c1)C(O)(C)C)O Request for Quotation
Chemical Name: [5-(2-hydroxypropan-2-yl)pyridin-3-yl]boronic acid
CAS Number: 1310404-56-8
Product Number: AG000VEY(AGN-PC-0ALTM5)
Synonyms:
MDL No:
Molecular Formula: C8H12BNO3
Molecular Weight: 180.9968

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(5-(2-Hydroxypropan-2-yl)pyridin-3-yl)boronic acid is a valuable reagent commonly used in organic synthesis as a boronic acid derivative. It serves as a versatile building block in the formation of carbon-carbon and carbon-heteroatom bonds in various chemical reactions. This compound is particularly important in Suzuki-Miyaura cross-coupling reactions, where it facilitates the coupling of aryl or vinyl halides with organic boronic acids under mild conditions to produce biaryl or alkenyl products. Additionally, (5-(2-Hydroxypropan-2-yl)pyridin-3-yl)boronic acid can be employed in the functionalization of aromatic compounds, heterocycles, and other organic molecules to introduce specific functional groups or substituents. Its unique structure and reactivity make it a valuable tool for synthetic chemists seeking to create complex molecular structures efficiently and selectively.