177035-82-4

Basic information

• Product Name: 1-Dodecylboronic acid pinacol
• Synonyms: 1-Dodecylboronic acid pinacol;1-Dodecylboronic acid pinacol ester, 98%
• CAS NO: 177035-82-4
• Molecular Formula: C₁₈H₃₇BO₂
• Molecular Weight: 296.299
• Mol File: 177035-82-4.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 123℃/0.2mm
• Appearance: /
• Density: 0.86±0.1 g/cm3(Predicted)
• Refractive Index: 1.4410
• CAS DataBase Reference: 1-Dodecylboronic acid pinacol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Dodecylboronic acid pinacol(177035-82-4)
• EPA Substance Registry System: 1-Dodecylboronic acid pinacol(177035-82-4)

Safety Data

• Hazardous Substances Data: 177035-82-4(Hazardous Substances Data)

Usage

Organic compound

1-Dodecylboronic acid pinacol is a carbon-containing compound, which is classified as an organic compound.

Boronic acid derivative

It is a derivative of boronic acid, which means it is a compound that contains a boron atom bonded to a hydroxyl group (-OH) and an organic group (in this case, a dodecyl group).

White solid

1-Dodecylboronic acid pinacol is a white solid, which means it has a solid form and a white color.

Building block in organic synthesis

It is commonly used in organic synthesis as a building block to form carbon-carbon and carbon-oxygen bonds, which means it is a useful compound for creating more complex molecules.

Utilized in production of pharmaceutical compounds, agrochemicals, and materials science

1-Dodecylboronic acid pinacol is used in the production of various compounds, including pharmaceuticals, agrochemicals, and materials.

Reagent in Suzuki-Miyaura coupling reactions

This chemical is often used as a reagent in Suzuki-Miyaura coupling reactions, which is a popular method for forming carbon-carbon bonds.

Exhibit antimicrobial and anticancer properties

1-Dodecylboronic acid pinacol has been found to exhibit antimicrobial and anticancer properties, which makes it a valuable compound in medicinal and pharmaceutical research.

Known for its hydrophobic properties

It is known for its hydrophobic properties, which means it is a compound that repels water, making it useful in surfactant and emulsifier formulations.

Upstream product

• 124-22-1 n-Dodecylamine 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 13826-27-2 2,2'-bis(1,3,2-benzodioxaborole) 
• 4292-19-7 1-Iodododecane 
• 112-40-3 dodecane 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 
• 143-15-7 1-dodecylbromide 
• 73183-34-3 bis(pinacol)diborane 
• 112-41-4 1-dodecene 
• 112-52-7 1-chlorododecane 

Downstream Products

• 3088-79-7 n-dodecylboronic acid 
• 112-41-4 1-dodecene 
• 112-40-3 dodecane 

Relevant articles and documents

Does Lewis basicity correlate with catalytic performance in zerovalent group 8 complexes?

A set of 18 zerovalent group 8 metal complexes of the form [MLn(CO)5-n] (M=Fe, Ru, Os; L=neutral donor; n=0-2) were screened for their catalytic performance in aldehyde hydrosilylation and olefin hydroboration reactions. Although none of the untested catalysts were found to perform better than the previously-published complex [Fe(CO)4(IMes)] (IMes=1,3-Dimesityliidazol-2-ylidene), the results suggest that the Lewis basicity of the metal complex does not play a critical role in the catalysis of these two reactions.

Ruthenium-Catalyzed Dehydrogenation Through an Intermolecular Hydrogen Atom Transfer Mechanism

The direct dehydrogenation of alkanes is among the most efficient ways to access valuable alkene products. Although several catalysts have been designed to promote this transformation, they have unfortunately found limited applications in fine chemical synthesis. Here, we report a conceptually novel strategy for the catalytic, intermolecular dehydrogenation of alkanes using a ruthenium catalyst. The combination of a redox-active ligand and a sterically hindered aryl radical intermediate has unleashed this novel strategy. Importantly, mechanistic investigations have been performed to provide a conceptual framework for the further development of this new catalytic dehydrogenation system.

Synthesis and Catalytic Reactivity of Cobalt Pincer Nitrosyl Hydride Complexes

The synthesis, characterization, and catalytic activity of low-spin {CoNO}8 pincer complexes of the type [Co(PCP)(NO)(H)] are described. These compounds are obtained either by reacting [Co(PCP)(κ2-BH4)] with NO and Et3N or, alternatively, by reacting [Co(