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1-Boc-pyrazole-4-boronic acid pinacol ester_Molecular_structure_CAS_)
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1-Boc-pyrazole-4-boronic acid pinacol ester

Catalog No. 632732 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C14H23BN2O4 Telephone 1-800-521-8956
M. W. 294.15442 Fax
Purity 97% Email
Storage Chembase ID: 67756

SYNONYMS

Title
1-Boc-吡唑-4-硼酸频哪醇酯
IUPAC name
tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate
IUPAC Traditional name
tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole-1-carboxylate
Synonyms
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole-1-carboxylic acid tert-butyl ester
tert-Butyl 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-pyrazolecarboxylate
4-(4,4,5,5-四甲基-1,3,2-二氧杂环硼戊烷-2-基)-1-吡唑羧酸叔丁酯
1-tert-Butoxycarbonyl-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)pyrazole
1,1-dimethylethyl ester 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-Pyrazole-1-carboxylic acid
1-Boc-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
[1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl]boronic acid pinacol ester
1-Boc-4-pyrazoleboronic acid pinacol ester
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-Boc-pyrazole
1-叔丁氧羰基-吡唑-4-硼酸频哪醇酯
4-(4,4,5,5-四甲基-1,3,2-二氧杂环硼戊烷-2-基)-1-Boc-吡唑

DATABASE IDS

PubChem SID 24882509
MDL Number MFCD05663873

PROPERTIES

Empirical Formula (Hill Notation) C14H23BN2O4
Purity 97%
Melting Point 82-86 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reagent used for
• Suzuki Coupling1
• Copper-catalyzed azidation2 Reagent used in Preparation of
• Selective quinazolinyl-phenol inhibitors of CHK1 as potential antitumors and radioprotectants3
• Stereoselective synthesis of selective Cathepsin inhibitors1
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reagent used for
• Suzuki Coupling1
• Copper-catalyzed azidation2 Reagent used in Preparation of
• Selective quinazolinyl-phenol inhibitors of CHK1 as potential antitumors and radioprotectants3
• Stereoselective synthesis of selective Cathepsin inhibitors1

REFERENCES