254892-99-4

Basic information

• Product Name: 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL
• Synonyms: 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL
• CAS NO: 254892-99-4
• Molecular Formula: C₁₂H₁₅BO₄
• Molecular Weight: 234.06
• Mol File: 254892-99-4.mol

Chemical Properties

• Boiling Point: 419.5 °C at 760 mmHg
• Flash Point: 207.5 °C
• Appearance: /
• Density: 1.29 g/cm³
• Vapor Pressure: 8.66E-08mmHg at 25°C
• Refractive Index: 1.581
• CAS DataBase Reference: 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL(254892-99-4)
• EPA Substance Registry System: 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL(254892-99-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 254892-99-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3-(4-Boronophenyl)cyclobutanone ethylene ketal is used as a synthetic intermediate for the creation of new chemical compounds. Its boron atom and ethylene ketal group provide unique reactivity, facilitating various chemical transformations and synthetic pathways.
Used in Materials Science:
In the field of materials science, 3-(4-Boronophenyl)cyclobutanone ethylene ketal is utilized for the development of novel materials. 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL's unique structure and reactivity can contribute to the design and synthesis of advanced materials with specific properties for various applications.
Used in Pharmaceutical Industry:
3-(4-Boronophenyl)cyclobutanone ethylene ketal is used as a building block in the pharmaceutical industry for the synthesis of potential drug candidates. Its unique chemical properties can be leveraged to create new molecules with therapeutic potential.
Used in Chemical Research:
In the realm of chemical research, 3-(4-Boronophenyl)cyclobutanone ethylene ketal serves as a subject of study to explore its reactivity and properties. Understanding its behavior in different chemical environments can lead to the discovery of new reactions and applications.

InChI:InChI=1/C12H15BO4/c14-13(15)11-3-1-9(2-4-11)10-7-12(8-10)16-5-6-17-12/h1-4,10,14-15H,5-8H2

Upstream product

• 254892-87-0 3-(4-bromophenyl)-2,2-dichlorocyclobutan-1-one 
• 254892-91-6 3-(4-bromophenyl)cyclobutanone 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 254892-95-0 3-(4-bromophenyl)cyclobutanone ethylene ketal 

Downstream Products

• 254893-07-7 C₁₂H₁₃BN₂O₄ 
• 254892-82-5 1-amino-3-(4-dihydroxyborylphenyl)cyclobutanecarboxylic acid 
• 254893-03-3 3-(4-boronophenyl)cyclobutanone 

Relevant articles and documents

4-Dihydroxyborylphenyl Analogues of 1-Aminocyclobutanecarboxylic Acids: Potential Boron Neutron Capture Therapy Agents

A series of 4-dihydroxyborylphenyl analogues of an unnatural α-amino acid, 1-aminocyclobutanecarboxylic acid (ACBC), was synthesized. Varying numbers of methylene units were introduced between the 4-boronophenyl and ACBC moieties in order to introduce different degrees of lipophilicity into the molecules. The key step in the syntheses was the preparation of the precursor p-boronophenyl-substituted cyclobutanones which were subsequently converted to the desired amino acids via the Bucherer-Strecker reaction.