233584-42-4

Basic information

• Product Name: (3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid
• Synonyms: (3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid;233584-42-4;(3,5-ditert-butyl-4-methoxyphenyl)boronic acid;Boronic acid, [3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]-;C15H25BO3;3,5-Di-tert-butyl-4-methoxy-phenylboronic acid;(3,5-Di-tert-butyl-4-methoxyphenyl)boronic acidE;(3,5-DI-TERT-BUTYL-4-METHOXYPHENYL) BORONIC ACID
• CAS NO: 233584-42-4
• Molecular Weight: 264.173
• Mol File: 233584-42-4.mol

Chemical Properties

• CAS DataBase Reference: (3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid(233584-42-4)
• EPA Substance Registry System: (3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid(233584-42-4)

Safety Data

• Hazardous Substances Data: 233584-42-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid is used as a reagent in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic compounds. It is a key intermediate in the production of various pharmaceuticals, pesticides, and materials used in the electronics industry.
Used in Organic Synthesis:
(3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid is used as a building block in organic synthesis for the creation of complex organic compounds.
Used in Pharmaceutical Research:
(3,5-Di-tert-butyl-4-methoxyphenyl)boronic acid is used as a subject of interest in pharmaceutical research due to its antioxidant and anti-inflammatory properties.

Upstream product

• 121-43-7 Trimethyl borate 
• 1516-96-7 4-bromo-2,6-di-tert-butylanisole 
• 7732-18-5 water 
• 1139-52-2 4-bromo-2,6-di-tert-butylphenol 
• 1016971-71-3 C₃₃H₄₅B₃O₁₀ 
• 1016971-69-9 C₃₉H₅₇B₃O₈ 
• 1016971-64-4 C₃₁H₄₁B₃O₄ 
• 1016971-63-3 C₃₈H₅₅B₃O₅ 
• 1016971-62-2 C₃₃H₄₅B₃O₆ 
• 1016971-61-1 C₃₉H₅₇B₃O₆ 
• 1016971-60-0 C₄₅H₆₉B₃O₆ 

Downstream Products

• 1016971-62-2 C₃₃H₄₅B₃O₆ 
• 1016971-61-1 C₃₉H₅₇B₃O₆ 
• 1016971-60-0 C₄₅H₆₉B₃O₆ 
• 34907-43-2 tris(4-methoxy-3.5-dimethyl phenyl)boroxine 
• 1016971-64-4 C₃₁H₄₁B₃O₄ 
• 1016971-63-3 C₃₈H₅₅B₃O₅ 
• 34907-38-5 tris(3.5-dimethyl phenyl)boroxine 
• 1016971-56-4 C₂₇H₃₃B₃O₁₂ 
• 1016971-71-3 C₃₃H₄₅B₃O₁₀ 
• 1016971-69-9 C₃₉H₅₇B₃O₈ 
• 1032358-19-2 2-[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 878269-53-5 2,9-bis-(3,5-di-tert-butyl-4-methoxyphenyl)-1,10-phenanthroline 
• 1606141-13-2 1-trifluoromethylthio-4-methoxy-3,5-di-tert-butylbenzene 

Relevant articles and documents

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Pyridinium phenolates possess a dissymmetric delocalised π-electron system providing a huge quadratic nonlinearity. They are a promising class of molecules for applications in photoelectronics and photonics. Semiempirical calculations indicate that the interplanar angle between the two aromatic rings leads to enhancement in the NLO properties of these compounds. The confirmation of this feature may be provided by the study of a new series of sterically hindered pyridinium phenolates 2a-e bearing two tert-butyl substituents at the ortho position(s) of the phenolate functionality. Such bulky groups would enhance the solubility of zwitterions in organic solvents and would limit the formation of aggregates. Their efficient preparations by using Suzuki cross-coupling reactions involving 3,5-dialkylated 4-bromopyridine N-oxides are described herein. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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