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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)-

1-methyl-4-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]piperazine

CN1CCN(CC1)Cc1ccc(cc1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1-methyl-4-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]piperazine
CAS Number: 938043-30-2
Product Number: AG0060M4(AGN-PC-07XU1J)
Synonyms:
MDL No:
Molecular Formula: C18H29BN2O2
Molecular Weight: 316.2461

Identification/Properties

Properties
MP:
61-65°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
316.252g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
316.232g/mol
Monoisotopic Mass:
316.232g/mol
Topological Polar Surface Area:
24.9A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
384
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]piperazine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This molecule serves as a valuable building block in the creation of diverse organic compounds due to its functional groups and structural features. In particular, it is commonly employed in the formation of complex pharmaceutical intermediates and fine chemicals through various synthetic routes. The presence of boron and the piperazine ring in its structure enhances its utility in organic transformations, such as cross-coupling reactions and nucleophilic substitutions, enabling the efficient construction of intricate molecular architectures. Additionally, the methyl substituents on the boron atom contribute to its stability and compatibility in a range of synthetic conditions. The strategic incorporation of 1-Methyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]piperazine in chemical synthesis endeavors enables chemists to access novel compounds and advance research in medicinal chemistry, materials science, and other interdisciplinary fields.