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N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester, 95%

CAS: 286961-14-6 | C16H28BNO4 | 309.21 g/mol

$144.59 - $1841.22

Chemical Identifiers

CAS 286961-14-6
Molecular Formula C16H28BNO4
Molecular Weight (g/mol) 309.21
MDL Number MFCD03840345
InChI Key VVDCRJGWILREQH-UHFFFAOYSA-N
Synonym n-boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester, tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-5,6-dihydropyridine-1 2h-carboxylate, 1-n-boc-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-3,6-dihydro-2h-pyridine, n-boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-3,6-dihydro-2h-pyridine-1-carboxylate, tert-butyl 5,6-dihydro-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl pyridine-1 2h-carboxylate, 3,6-dihydro-2h-pyridine-1-n-boc-4-boronic acid pinacol ester, n-tert-butoxycarbonyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, 1-boc-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-3,6-dihydro-2h-pyridine, tert-butyl 4-tetramethyl-1,3,2-dioxaborolan-2-yl-1,2,3,6-tetrahydropyridine-1-carboxylate
PubChem CID 4642098
IUPAC Name tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate
SMILES CC(C)(C)OC(=O)N1CCC(=CC1)B1OC(C)(C)C(C)(C)O1
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AAH6619303
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H6619303
1 g
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AAH6619306
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H6619306
5 g
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AAH6619314
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Description

Description

Reagent used for suzuki-Miyaura cross-coupling using palladium phosphine catalyst, palladium-catalyzed ligand-controlled regioselective Suzuki coupling, wrenchnolol derivative optimized for gene activation in cells. Also used in Preparation of several enzymatic inhibitors and receptor ligands, orally active anaplastic lymphoma kinase inhibitors and oxazolecarboxamides as diacylglycerol acyltransferase-1 inhibitors for treatment of obesity and diabetes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Reagent used for suzuki-Miyaura cross-coupling using palladium phosphine catalyst, palladium-catalyzed ligand-controlled regioselective Suzuki coupling, wrenchnolol derivative optimized for gene activation in cells. Also used in Preparation of several enzymatic inhibitors and receptor ligands, orally active anaplastic lymphoma kinase inhibitors and oxazolecarboxamides as diacylglycerol acyltransferase-1 inhibitors for treatment of obesity and diabetes.

Solubility
Soluble in most organic solvents. Insoluble in water.

Notes
Store in cool, dry place in tightly closed container. With adequate ventilation. Store away from oxidizing agent.
Specifications

Chemical Identifiers

286961-14-6
309.21
VVDCRJGWILREQH-UHFFFAOYSA-N
4642098
CC(C)(C)OC(=O)N1CCC(=CC1)B1OC(C)(C)C(C)(C)O1
C16H28BNO4
MFCD03840345
n-boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester, tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-5,6-dihydropyridine-1 2h-carboxylate, 1-n-boc-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-3,6-dihydro-2h-pyridine, n-boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-3,6-dihydro-2h-pyridine-1-carboxylate, tert-butyl 5,6-dihydro-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl pyridine-1 2h-carboxylate, 3,6-dihydro-2h-pyridine-1-n-boc-4-boronic acid pinacol ester, n-tert-butoxycarbonyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, 1-boc-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-3,6-dihydro-2h-pyridine, tert-butyl 4-tetramethyl-1,3,2-dioxaborolan-2-yl-1,2,3,6-tetrahydropyridine-1-carboxylate
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate

Specifications

286961-14-6
MFCD03840345
n-boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester, tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-5,6-dihydropyridine-1 2h-carboxylate, 1-n-boc-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-3,6-dihydro-2h-pyridine, n-boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, tert-butyl 4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-3,6-dihydro-2h-pyridine-1-carboxylate, tert-butyl 5,6-dihydro-4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl pyridine-1 2h-carboxylate, 3,6-dihydro-2h-pyridine-1-n-boc-4-boronic acid pinacol ester, n-tert-butoxycarbonyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, 1-boc-4-4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl-3,6-dihydro-2h-pyridine, tert-butyl 4-tetramethyl-1,3,2-dioxaborolan-2-yl-1,2,3,6-tetrahydropyridine-1-carboxylate
VVDCRJGWILREQH-UHFFFAOYSA-N
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate
4642098
95%
N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester
C16H28BNO4
1 g
Soluble in most organic solvents. Insoluble in water.
CC(C)(C)OC(=O)N1CCC(=CC1)B1OC(C)(C)C(C)(C)O1
309.21
327.23
Solid
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Safety and Handling

Safety and Handling

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only