1029438-14-9

Basic information

• Product Name: 4'-Acetylbiphenyl-4-boronic acid
• Synonyms: 4'-Acetylbiphenyl-4-boronic acid;(4'-Acetyl-[1,1'-biphenyl]-4-yl)boronic acid
• CAS NO: 1029438-14-9
• Molecular Formula: C₁₄H₁₃BO₃
• Molecular Weight: 240.06222
• Mol File: 1029438-14-9.mol

Chemical Properties

• Boiling Point: 441.5±47.0 °C(Predicted)
• Appearance: /
• Density: 1.22±0.1 g/cm3(Predicted)
• Storage Temp.: Room temperature.
• PKA: 8.46±0.17(Predicted)
• CAS DataBase Reference: 4'-Acetylbiphenyl-4-boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-Acetylbiphenyl-4-boronic acid(1029438-14-9)
• EPA Substance Registry System: 4'-Acetylbiphenyl-4-boronic acid(1029438-14-9)

Safety Data

• Hazardous Substances Data: 1029438-14-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4'-Acetylbiphenyl-4-boronic acid is used as a starting material for the synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a promising candidate for the development of new drugs with potential therapeutic applications.
In Organic Synthesis:
4'-Acetylbiphenyl-4-boronic acid is used as a building block in organic synthesis for the preparation of various organic compounds. Its increased reactivity due to the acetyl group on the biphenyl ring allows for efficient cross-coupling reactions, facilitating the synthesis of complex organic molecules.
In Suzuki Coupling Reactions:
4'-Acetylbiphenyl-4-boronic acid is used as a reactant in Suzuki coupling reactions, a type of cross-coupling reaction used to form carbon-carbon bonds. Its ability to form stable complexes with diols makes it a suitable choice for this reaction, enabling the formation of biaryl compounds with potential applications in various fields.
In Other Organic Transformations:
Due to its reactivity and ability to form stable complexes, 4'-Acetylbiphenyl-4-boronic acid can be employed in various other organic transformations, such as the synthesis of heterocycles, natural products, and other complex organic molecules. Its versatility in organic synthesis makes it a valuable tool for chemists working in different areas of research.

Downstream Products

• 1354627-15-8 (4S,5R,6S)-3-(4'-acetyl-biphenyl-4-yl)-4-methyl-7-oxo-6-((1'R)-triethylsilanyloxy-ethyl)-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl-ester 

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.

INHIBITORS OF FATTY ACID AMIDE HYDROLASE

The present invention provide compounds, and pharmaceutical compositions thereof, encompassed by the formulae (I), (II) or (III). The present invention also provides methods for treating FAAH mediated disease, disorder or condition by administering a ther