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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)-

6-Chloro-5-methylpyridine-3-boronic acid pinacol ester

Clc1ncc(cc1C)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 6-Chloro-5-methylpyridine-3-boronic acid pinacol ester
CAS Number: 1010101-07-1
Product Number: AG0003IA(AGN-PC-0OQ9UZ)
Synonyms:
MDL No:
Molecular Formula: C12H17BClNO2
Molecular Weight: 253.5329

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
253.533g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
253.104g/mol
Monoisotopic Mass:
253.104g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
282
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-3-methylpyridine-5-boronic Acid Pinacol Ester is a versatile compound commonly used in chemical synthesis as a valuable building block. It serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and materials. This compound is particularly prized for its ability to introduce the boronic acid functionality into organic molecules, allowing for further derivatization and functionalization through classic cross-coupling reactions such as Suzuki-Miyaura coupling. Its unique structure and reactivity make it an essential tool for organic chemists seeking to create complex molecular structures with precision and efficiency.