N-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester

• Catalog No.: 706531
• CAS Number: 286961-14-6
• M. F.: C16H28BNO4
• M. W.: 309.20882
• Purity: 95%

SYNONYMS

• Title: N-Boc-1,2,3,6-四氢吡啶-4-硼酸频哪醇酯
• IUPAC name: tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate
• IUPAC Traditional name: tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate
• Synonyms: (N-tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester; (N-叔丁氧羰基)-1,2,3,6-四氢吡啶-4-硼酸频哪醇酯; (1-tert-Butoxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)boronic acid pinacol ester; (N-tert-Butoxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)boronic acid pinacol ester; (N-tert-Butoxycarbonyl-1,2,5,6-tetrahydropyridin-4-yl)boronic acid pinacol ester

DATABASE IDS

• CAS Number: 286961-14-6
• MDL Number: MFCD03840345

PROPERTIES

• Empirical Formula (Hill Notation): C16H28BNO4
• Purity: 95%
• Melting Point: 100-114 °C
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
250 mg in glass bottle
Application
Reagent used for
• Suzuki-Miyaura cross-coupling using palladium phosphine catalyst1
• Palladium-catalyzed ligand-controlled regioselective Suzuki coupling2
• Palladium-catalyzed Suzuki-Miyaura coupling3
• Suzuki coupling followed by iodolactonization reaction4
• Wrenchnolol derivative optimized for gene activation in cells5 Reagent used in Preparation of several enzymatic inhibitors and receptor ligands
• Orally active anaplastic lymphoma kinase inhibitors6
• Oxazolecarboxamides as diacylglycerol acyltransferase-1 inhibitors for treatment of obesity and diabetes7
• 4-arylpiperidinyl amides and N-arylpiperidin-3-yl-cyclopropanecarboxamides as novel melatonin receptor ligands8
• Quinazoline analogs as glucocerebrosidase inhibitors with chaperone activity for treatment of Gaucher disease, a lysosomal storage disorder9
• Arylpiperazine and piperidine ethers as dual acting norepinephrine reuptake inhibitors and 5-HT1A partial agonists10

Description (简体中文)

包装
1 g in glass bottle
250 mg in glass bottle
Application
Reagent used for
• Suzuki-Miyaura cross-coupling using palladium phosphine catalyst1
• Palladium-catalyzed ligand-controlled regioselective Suzuki coupling2
• Palladium-catalyzed Suzuki-Miyaura coupling3
• Suzuki coupling followed by iodolactonization reaction4
• Wrenchnolol derivative optimized for gene activation in cells5 Reagent used in Preparation of several enzymatic inhibitors and receptor ligands
• Orally active anaplastic lymphoma kinase inhibitors6
• Oxazolecarboxamides as diacylglycerol acyltransferase-1 inhibitors for treatment of obesity and diabetes7
• 4-arylpiperidinyl amides and N-arylpiperidin-3-yl-cyclopropanecarboxamides as novel melatonin receptor ligands8
• Quinazoline analogs as glucocerebrosidase inhibitors with chaperone activity for treatment of Gaucher disease, a lysosomal storage disorder9
• Arylpiperazine and piperidine ethers as dual acting norepinephrine reuptake inhibitors and 5-HT1A partial agonists10