1,3,5-Phenyltriboronic acid, pinacol ester - Names and Identifiers
Name | 1,3,2-Dioxaborolane, 2,2',2''-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl-
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Synonyms | 1,3,5-Phenyltriboronic acid, pinacol ester 1,3,5-Benzenetriboronic Acid Tris(pinacol) Ester benzene-1,3,5-triyltriboronic acid pinacol ester 1,3,5-Phenyltriboronicacid,Tris(Pinacol)Esteraldrichcpr 1,3,5-Tris(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzene 1,3,2-Dioxaborolane, 2,2',2''-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl- 2-[3,5-Bis(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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CAS | 365564-05-2
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1,3,5-Phenyltriboronic acid, pinacol ester - Physico-chemical Properties
Molecular Formula | C24H39B3O6
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Molar Mass | 455.996 |
Density | 1.05±0.1 g/cm3(Predicted) |
Melting Point | 286-287°C |
Boling Point | 555.6±45.0 °C(Predicted) |
Appearance | Morphological powder or crystals |
Storage Condition | Inert atmosphere,Room Temperature |
1,3,5-Phenyltriboronic acid, pinacol ester - Upstream Downstream Industry
1,3,5-Phenyltriboronic acid, pinacol ester - Introduction
1,3,2-Dioxaborolane, 2,2 ',2 "-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl-(1,3,5-Phenylboronic acid trineopentanol ester) is an organic compound with the chemical formula C21H27BO6.
Nature:
1,3,2-Dioxaborolane, 2,2 ',2 ''-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl-is a white solid that may appear crystalline. It is soluble in organic solvents such as methanol, ethanol or dichloromethane, but poorly soluble in water.
Use:
1,3,2-Dioxaborolane, 2,2 ',2 ''-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl-is an important organic synthesis intermediate, widely used in catalytic reduction, coupling reaction and Cross-Coupling reaction. It can be used to prepare organic compounds such as pharmaceuticals, pesticides and functional materials.
Preparation Method:
a common method for preparing 1,3,2-Dioxaborolane, 2,2 ',2 ''-(1,3,5-benzenetriyl)tris[4,4,5,5, 5-tetramethyl -1,3, 2-diboron is first reduced to 2,2',2''-(1,3,5-benzene triboronic acid triyl) three-frequency na alcohol. 1,3, 5-Benzenetriboronic acid triyltrinalactone was then reacted with an appropriate amount of carbon tetrachloride under an inert atmosphere to give the desired 1,3,2-Dioxaborolane, 2,2 ',2 "-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl-.
Safety Information:
Detailed safety information for
1,3,2-Dioxaborolane, 2,2 ',2 ''-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl-is not available. However, when handling organic compounds, it is generally necessary to pay attention to safe operation, use appropriate protective measures, such as wearing gloves and protective glasses, and operate in a well-ventilated area. When using the compound, relevant safety procedures should be followed and care should be taken to prevent contact with skin, eyes and respiratory tract.
Last Update:2024-04-09 02:00:46