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1-N-Boc-piperidine-4-boronicacidpinacolester, 98%|186183|1048970-17-7

1-N-Boc-piperidine-4-boronicacidpinacolester, 98%

Cat. No JK186183_5_G
J&K Chemical

Product Information

Product Name
1-N-Boc-piperidine-4-boronicacidpinacolester, 98%
Brand Name
J&K
Product Number
186183
CAS
1048970-17-7
Molecular Formula
C16H30BNO4
Molecular Weight
311.22
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate
PubChem CID
43811073
IUPAC Name
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate
InChI Key
IBLQMWKHENBVJE-UHFFFAOYSA-N
SMILES
B1(OC(C(O1)(C)C)(C)C)C2CCN(CC2)C(=O)OC(C)(C)C

Properties

Density
1.03
Melting Point
60-65
Boiling Point
358.8

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
H336
Precautionary Statement
P280
P305+P351+P338
P264+P265
P337+P317
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Iron-Catalyzed Borylation and Silylation of Alkyl Electrophiles
Publication Name: Science of Synthesis
Publication Date: 2023

Pyridine-Mediated B–B Bond Activation of (RO)2B–B(OR)2 for Generating Borylpyridine Anions and Pyridine-Stabilized Boryl Radicals as Useful Boryl Reagents in Organic Synthesis
Publication Name: Synthesis
Publication Date: 2021-05-25
DOI: 10.1055/a-1486-8169

Photoredox-Catalyzed Radical Addition–Polar Cyclization
Publication Name: Science of Synthesis
Publication Date: 2021

Radical Deoxygenative Borylation
Publication Name: Science of Synthesis
Publication Date: 2021

Radical Deaminative Borylation
Publication Name: Science of Synthesis
Publication Date: 2021

1-N-Boc-piperidine-4-boronicacidpinacolester, 98%

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