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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-benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine

CC1(C)OB(OC1(C)C)C1=CCCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 1-benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine
CAS Number: 1313738-80-5
Product Number: AG000W0X(AGN-PC-086EFY)
Synonyms:
MDL No:
Molecular Formula: C18H26BNO2
Molecular Weight: 299.2155

Identification/Properties

Computed Properties
Molecular Weight:
299.221g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
299.206g/mol
Monoisotopic Mass:
299.206g/mol
Topological Polar Surface Area:
21.7A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
411
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-H413
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine, commonly referred to as $name$, is a versatile compound predominantly used in chemical synthesis. This compound plays a crucial role as a key building block in the construction of complex organic molecules through various synthetic methodologies. Its unique structure and reactivity make it an essential component in the synthesis of pharmaceuticals, agrochemicals, and materials with diverse applications. The presence of both boron and nitrogen functionalities in $name$ enables it to participate in important organic reactions, such as Suzuki-Miyaura cross-coupling, palladium-catalyzed C-N bond formation, and C-H activation processes. These reactions facilitate the efficient assembly of structurally intricate molecules with high precision and selectivity. Additionally, the tetrahydropyridine moiety in $name$ imparts additional stereochemistry and functionality to the target molecules, enhancing their biological activity and physical properties. Overall, the strategic incorporation of 1-Benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine in chemical synthesis enables the synthesis of diverse compounds with synthetic efficiency and molecular complexity.