1. Home
  2. 6-Acetamidopyridine-3-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)-

6-Acetamidopyridine-3-boronic acid

CC(=O)Nc1ccc(cn1)B(O)O Request for Quotation
Chemical Name: 6-Acetamidopyridine-3-boronic acid
CAS Number: 947533-21-3
Product Number: AG00IIIG(AGN-PC-07B7CH)
Synonyms:
MDL No:
Molecular Formula: C7H9BN2O3
Molecular Weight: 179.9690

Identification/Properties

Computed Properties
Molecular Weight:
179.97g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
180.071g/mol
Monoisotopic Mass:
180.071g/mol
Topological Polar Surface Area:
82.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
189
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:
H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Boronic acid, B-[6-(acetylamino)-3-pyridinyl], is a versatile compound commonly used in chemical synthesis for its unique properties. This specific boronic acid derivative is particularly valuable due to its ability to participate in various organic reactions, making it a valuable tool in the preparation of complex molecules.One of the key applications of this compound is in Suzuki-Miyaura cross-coupling reactions, where it serves as a crucial component in the formation of carbon-carbon bonds. This reaction is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science, enabling chemists to efficiently construct intricate molecular structures.Furthermore, the boronic acid functionality in this compound can also undergo further transformations, such as oxidation or reduction, to introduce additional functional groups into the molecule. This flexibility allows for the synthesis of diverse compounds with tailored properties and functionalities.Overall, Boronic acid, B-[6-(acetylamino)-3-pyridinyl], plays a vital role in modern organic chemistry, facilitating the development of new materials, pharmaceuticals, and other valuable compounds through its participation in a range of synthetic pathways.