Description
1-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine (CAS: 1048976-83-5) is a high-purity boronic ester derivative with the molecular formula C18H26BNO2. This compound is a valuable synthetic intermediate, widely used in Suzuki-Miyaura cross-coupling reactions due to its stable pinacol boronate group. The benzyl-substituted tetrahydropyridine core enhances its reactivity in transition-metal-catalyzed transformations, making it ideal for constructing complex heterocyclic scaffolds in pharmaceutical and agrochemical research. Supplied as a crystalline solid, it is rigorously tested for purity (typically ≥95% by HPLC) and stored under inert conditions to ensure stability. Suitable for use in organic synthesis, medicinal chemistry, and material science applications.
Properties
- CAS Number: 1048976-83-5
- Complexity: 411
- IUPAC Name: 1-benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine
- InChI: InChI=1S/C18H26BNO2/c1-17(2)18(3,4)22-19(21-17)16-10-12-20(13-11-16)14-15-8-6-5-7-9-15/h5-10H,11-14H2,1-4H3
- InChI Key: SBZWAVVCJBBNSM-UHFFFAOYSA-N
- Exact Mass: 299.2056592
- Molecular Formula: C18H26BNO2
- Molecular Weight: 299.2
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CCN(CC2)CC3=CC=CC=C3
- Topological: 21.7
- Monoisotopic Mass: 299.2056592
- Synonyms: 1048976-83-5, 1-BENZYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1,2,3,6-TETRAHYDROPYRIDINE, 1-Benzyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, MFCD11501654, 1-benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine, SCHEMBL9952926, DTXSID80678049, SBZWAVVCJBBNSM-UHFFFAOYSA-N, (1-BENZYL-1,2,3,6-TETRAHYDROPYRIDIN-4-YL)BORONIC ACID PINACOL ESTER, AKOS015949248, CS-W001285, SB30375, 1,2,3,6-Tetrahydro-1-(phenylmethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, DS-13192, SY031554, DB-059223, 1-Benzyl-1,2,3,6-tetrahydropyridine-4-boronic acid, pinacol ester, 1-Benzyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1,2,3,6-tetrahydro-pyridine, 1-Benzyl-4-(4 pound not4 pound not5 pound not5-tetramethyl-1 pound not3 pound not2-dioxaborolan-2-yl)-1 pound not2 pound not3 pound not6-tetrahydropyridine
Application
This compound is primarily employed as a key intermediate in palladium-catalyzed cross-coupling reactions, enabling the synthesis of biaryl and heteroaryl structures. Researchers utilize it in the development of pharmaceutical candidates, particularly for CNS-targeting molecules due to its benzyl-tetrahydropyridine moiety. It also serves as a precursor for boronic acid derivatives in sensor and polymer chemistry.
If you are interested or have any questions, please contact us at support@atomfair.com
Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


Reviews
There are no reviews yet.