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4-Nitrophenylboronic acid pinacol ester_Molecular_structure_CAS_171364-83-3)
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4-Nitrophenylboronic acid pinacol ester

Catalog No. 643890 Name Sigma Aldrich
CAS Number 171364-83-3 Website http://www.sigmaaldrich.com
M. F. C12H16BNO4 Telephone 1-800-521-8956
M. W. 249.07074 Fax
Purity Email
Storage Chembase ID: 12420

SYNONYMS

Title
4-硝基苯硼酸频哪醇酯
IUPAC name
4,4,5,5-tetramethyl-2-(4-nitrophenyl)-1,3,2-dioxaborolane
IUPAC Traditional name
4,4,5,5-tetramethyl-2-(4-nitrophenyl)-1,3,2-dioxaborolane
Synonyms
4-(4,4,5,5-四甲基-1,3,2-二氧杂戊硼烷-2-基)硝基苯
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene

DATABASE IDS

PubChem SID 24883300
MDL Number MFCD02179437
CAS Number 171364-83-3

PROPERTIES

Empirical Formula (Hill Notation) C12H16BNO4
Melting Point 112-116 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reactant involved in:
• Synthesis of aryl azides 1
• Arylation of allylic chlorides2
• Syntehsis of RNA conjugates3
• Alkoxycarbonylation4
• Synthesis of mTOR and PI3K inhibitors as antitumor agents5
• Electrooxidative synthesis of biaryls6
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant involved in:
• Synthesis of aryl azides 1
• Arylation of allylic chlorides2
• Syntehsis of RNA conjugates3
• Alkoxycarbonylation4
• Synthesis of mTOR and PI3K inhibitors as antitumor agents5
• Electrooxidative synthesis of biaryls6

REFERENCES