1. Home
  2. 3-Chloro-2-methoxypyridine-5-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)-

3-Chloro-2-methoxypyridine-5-boronic acid

COc1ncc(cc1Cl)B(O)O Request for Quotation
Chemical Name: 3-Chloro-2-methoxypyridine-5-boronic acid
CAS Number: 942438-89-3
Product Number: AG006CWM(AGN-PC-04TKR6)
Synonyms:
MDL No:
Molecular Formula: C6H7BClNO3
Molecular Weight: 187.3887

Identification/Properties

Properties
BP:
337.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
187.386g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
187.021g/mol
Monoisotopic Mass:
187.021g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
149
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#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Chloro-2-methoxypyridine-5-boronic acid is a versatile compound widely used in chemical synthesis as a key building block for the development of various pharmaceuticals, agrochemicals, and materials. Its unique structure and properties make it a valuable intermediate in the creation of a wide range of functional molecules.In chemical synthesis, 3-Chloro-2-methoxypyridine-5-boronic acid serves as a crucial component in the construction of complex organic compounds through Suzuki-Miyaura cross-coupling reactions. By leveraging its boronic acid group, this compound can effectively participate in palladium-catalyzed coupling reactions with aryl halides or triflates, facilitating the formation of new carbon-carbon bonds.Furthermore, the presence of the chloro and methoxy substituents on the pyridine ring enables precise manipulation of the compound's reactivity and selectivity in various synthetic pathways. These functional groups can undergo further derivatization to introduce additional chemical functionalities, allowing for the tailored synthesis of target molecules with specific properties and activities.Overall, 3-Chloro-2-methoxypyridine-5-boronic acid plays a crucial role in modern chemical synthesis by enabling the efficient and controlled construction of diverse organic compounds, making it an essential tool for researchers and chemists in the development of novel pharmaceuticals, agrochemicals, and materials.