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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)-

2-(Piperazin-1-yl)pyridine-4-boronic acid, pinacol ester

CC1(C)OB(OC1(C)C)c1ccnc(c1)N1CCNCC1 Request for Quotation
Chemical Name: 2-(Piperazin-1-yl)pyridine-4-boronic acid, pinacol ester
CAS Number: 957198-31-1
Product Number: AG003F47(AGN-PC-0WA5DX)
Synonyms:
MDL No:
Molecular Formula: C15H24BN3O2
Molecular Weight: 289.1810

Identification/Properties

Properties
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
289.186g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
289.196g/mol
Monoisotopic Mass:
289.196g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
356
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine is a versatile compound commonly employed in chemical synthesis as a key building block. Through its intricate molecular structure, this compound acts as a valuable reagent in the preparation of various functionalized organic molecules. Its unique properties enable it to participate in a wide range of synthetic reactions, facilitating the creation of complex organic frameworks with enhanced structural diversity. By serving as a pivotal intermediate in synthetic pathways, 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine plays a crucial role in the efficient and strategic synthesis of biologically active compounds, pharmaceuticals, and advanced materials. Its utility in chemical synthesis underscores its significance as a sophisticated tool for the construction of novel molecular architectures.