(2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid is a boronic acid derivative characterized by a molecular formula of C12H19BO4Si. It features a bulky tert-butyldimethylsilyloxyphenyl group attached to the boron center, which provides protection for the boronic acid functionality and allows for selective reactions at other sites within a molecule. (2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid is a versatile tool in organic synthesis, enabling the creation of various biaryl compounds and participation in a range of chemical transformations.
929277-63-4
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Basic information
- Product Name: 2-(tert-Butyldimethylsilyloxy)phenylboronic acid
- Synonyms: 2-(tert-Butyldimethylsilyloxy)phenylboronic acid
- CAS NO:929277-63-4
- Molecular Formula: C12H21BO3Si
- Molecular Weight: 252.18984
- EINECS: N/A
- Product Categories: N/A
- Mol File: 929277-63-4.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
- Solubility: N/A
- CAS DataBase Reference: 2-(tert-Butyldimethylsilyloxy)phenylboronic acid(CAS DataBase Reference)
- NIST Chemistry Reference: 2-(tert-Butyldimethylsilyloxy)phenylboronic acid(929277-63-4)
- EPA Substance Registry System: 2-(tert-Butyldimethylsilyloxy)phenylboronic acid(929277-63-4)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 929277-63-4(Hazardous Substances Data)
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929277-63-4 Usage
Uses
Used in Organic Synthesis:(2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid is used as a building block for the creation of various biaryl compounds. Its bulky tert-butyldimethylsilyl group offers protection for the boronic acid functionality, enabling selective reactions to occur at other sites within a molecule.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic synthesis, (2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid serves as a reagent for Suzuki-Miyaura cross-coupling reactions. This reaction is a widely used method for the formation of carbon-carbon bonds, particularly in the synthesis of biaryl compounds, which are important structural motifs in pharmaceuticals, agrochemicals, and materials science.
Used in the Construction of Complex Organic Molecules:
The boronic acid moiety in (2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid allows (2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid to participate in various chemical transformations, making it a valuable tool for the construction of complex organic molecules. Its versatility in organic synthesis contributes to the development of new compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 929277-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,2,7 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.Calculate Digit Verification of CAS Registry Number 929277-63:
(8*9)+(7*2)+(6*9)+(5*2)+(4*7)+(3*7)+(2*6)+(1*3)=214
214 % 10 = 4
So 929277-63-4 is a valid CAS Registry Number.
929277-63-4Upstream product
929277-63-4Downstream Products
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2-(tert-Butyldimethylsilyloxy)phenylboronic acid
