1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1Z)-2-phenylethenyl]- - Names and Identifiers
Name | (Z)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane
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Synonyms | (Z)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1Z)-2-phenylethenyl]-
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CAS | 74213-48-2
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1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1Z)-2-phenylethenyl]- - Physico-chemical Properties
Molecular Formula | C14H19BO2
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Molar Mass | 230.11 |
Storage Condition | 2-8°C |
1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1Z)-2-phenylethenyl]- - Upstream Downstream Industry
1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1Z)-2-phenylethenyl]- - Introduction
(Z)-4,4,5,5-tetramethyl-2-styryl-1, 3,2-dioxaborane ((Z)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane) is an organic compound. Its chemical formula is C12H15BO2 and its molecular weight is 201.05g/mol.
This compound has the following properties:
1. Appearance: colorless to light yellow solid
2. Melting Point: about 60-70 ° C
3. Boiling point: About 200 ° C
4. Density: about 1.00 g/mL
5. Solubility: soluble in common organic solvents, and low solubility in water.
(Z)-4,4,5,5-tetramethyl -2-styryl-1, 3,2-dioxaborane is commonly used as a reagent in organic synthesis, it is used to construct carbon-boron bonds and other organic synthesis reactions. Due to its special structure and reactivity, it has a wide range of applications in synthetic chemistry.
The compound can be prepared by a lamination reaction (Grignard reaction). Typically, phenyl and methylene chloride methyl magnesium lithium are reacted with trichloroborane and selectively methylated.
With regard to safety information, a specific safety assessment cannot be provided due to limited information. However, in theory, for any chemical, follow proper laboratory procedures and read and understand the relevant safety data sheets and guidelines before use. Avoid direct contact with skin and eyes, and make sure to operate in a well-ventilated area.
Last Update:2024-04-10 22:29:15