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| | 4-Nitrophenylboronic acid pinacol ester Basic information |
| Product Name: | 4-Nitrophenylboronic acid pinacol ester | | Synonyms: | 4-NITROPHENYLBORONIC ACID PINACOL ESTER;4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)NITROBENZENE;4-Nitrobenzeneboronic acid, pinacol ester;4,4,5,5-tetramethyl-2-(4-nitrophenyl)-1,3,2-dioxaborolane;2-(4-Nitrophenyl)-4,4,5,5,-tetramethyl-1,3,2-dioxaborolane, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene;1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(4-nitrophenyl)-;4-Nitrophenylboronic acid pinacol ester
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene;-Nitrophenylboronic acid pinacol ester | | CAS: | 171364-83-3 | | MF: | C12H16BNO4 | | MW: | 249.07 | | EINECS: | | | Product Categories: | Aryl Boronate Esters;Boronate Esters;Boronic Acids and Derivatives;Chemical Synthesis;Organometallic Reagents;Aryl;Boronic ester;Organoborons;blocks;BoronicAcids;NitroCompounds;Pyrimidines | | Mol File: | 171364-83-3.mol |  |
| | 4-Nitrophenylboronic acid pinacol ester Chemical Properties |
| Melting point | 112-116 °C (lit.) | | Boiling point | 357.5±25.0 °C(Predicted) | | density | 1.14±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | powder or crystals | | color | White to Orange to Green | | Water Solubility | Slightly soluble in water. | | CAS DataBase Reference | 171364-83-3(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 2 | | Hazard Note | Harmful/Store Cold | | HazardClass | IRRITANT | | HS Code | 29333990 |
| | 4-Nitrophenylboronic acid pinacol ester Usage And Synthesis |
| Chemical Properties | White solid | | Uses | 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 | | Uses | 4-Nitrobenzeneboronic acid pinacol ester is a reactant involved in synthesis of aryl azides, arylation of allylic chlorides, synthesis of RNA conjugates, alkoxycarbonylation, synthesis of mTOR and PI3K inhibitors as antitumor agents, electro oxidative synthesis of biaryls. | | Uses | suzuki reaction | | Synthesis Reference(s) | The Journal of Organic Chemistry, 60, p. 7508, 1995 DOI: 10.1021/jo00128a024 |
| | 4-Nitrophenylboronic acid pinacol ester Preparation Products And Raw materials |
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