393870-04-7

Basic information

• Product Name: 4'-Methyl-4-biphenylboronic acid
• Synonyms: B-(4'-Methyl[1,1'-biphenyl]-4-yl)- Boronic acid;Boronic acid, (4'-Methyl[1,1'-biphenyl]-4-yl)-;[4-(4-Methylphenyl)phenyl]boronic acid;(4'-Methyl-[1,1'-biphenyl]-4-yl)boronic acid
• CAS NO: 393870-04-7
• Molecular Formula: C13H13BO2
• Molecular Weight: 212.05212
• Mol File: 393870-04-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 138 °C
• Boiling Point: 393.8±45.0 °C(Predicted)
• Appearance: /
• Density: 1.15±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.62±0.17(Predicted)
• CAS DataBase Reference: 4'-Methyl-4-biphenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-Methyl-4-biphenylboronic acid(393870-04-7)
• EPA Substance Registry System: 4'-Methyl-4-biphenylboronic acid(393870-04-7)

Safety Data

• Hazardous Substances Data: 393870-04-7(Hazardous Substances Data)

Usage

General Description

4'-Methyl-4-biphenylboronic acid is a chemical compound belonging to the class of biphenylboronic acids. It is a boronic acid derivative with a methyl group attached to the 4' position of one of the biphenyl rings. 4'-Methyl-4-biphenylboronic acid is commonly used in organic synthesis as a reagent for coupling reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is also utilized in the production of pharmaceuticals, agrochemicals, and materials science. 4'-Methyl-4-biphenylboronic acid is a useful tool in the development of new molecules and materials due to its ability to participate in a variety of chemical transformations.

Upstream product

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Relevant articles and documents

1, 3, 5 - cyclohexanetriol - cis - or organic boronic acid-stable siloxy inositol complex and organic synthetic reaction using a reagent art

PROBLEM TO BE SOLVED: To provide a stable ate-type complex of an organoboronic acid as a reagent for organic synthesis reaction; and manufacturing techniques thereof.SOLUTION: A stable ate-type complex of an organoboronic acid with scyllo-inositol or 1,3,5-cis-cyclohexanetriol comprises an anion represented by the specified general formula (I) or (II) as a constituent. In the formula, Rand Reach represent an alkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group or aralkyl group which may have substituents.

B-protected haloboronic acids for iterative cross-coupling

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A simple and modular strategy for small molecule synthesis: Iterative Suzuki-Miyaura coupling of B-protected haloboronic acid building blocks

We herein describe a simple and highly modular strategy for small molecule synthesis involving the iterative cross-coupling of B-protected bifunctional haloboronic acids. Enabling this approach, we have newly discovered that the pyramidalization of boroni