389621-83-4

Basic information

• Product Name: 4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID
• Synonyms: 4-(PIPERIDINE-1-CARBONYL)BENZENEBORONIC ACID;4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID;4-(1-PIPERIDINYLCARBONYL)PHENYLBORONIC ACID;N-PIPERIDINYL 4-BORONOBENZAMIDE;4-(Piperidin-1-ylcarbonyl)benzeneboronic acid;Boronic acid, [4-(1-piperidinylcarbonyl)phenyl]- (9CI);(4-boronophenyl)(piperidin-1-yl)methanone;1-(4-Boronobenzoyl)piperidine
• CAS NO: 389621-83-4
• Molecular Formula: C₁₂H₁₆BNO₃
• Molecular Weight: 233.07
• Product Categories: BORONICACID;blocks;BoronicAcids;Aryl;Organoborons;Boronic acid;Boronate Ester;Potassium Trifluoroborate
• Mol File: 389621-83-4.mol

Chemical Properties

• Melting Point: 150-154°C
• Boiling Point: 456.1 °C at 760 mmHg
• Flash Point: 229.6 °C
• Appearance: /
• Density: 1.22g/cm³
• Vapor Pressure: 4.12E-09mmHg at 25°C
• Refractive Index: 1.577
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID(389621-83-4)
• EPA Substance Registry System: 4-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID(389621-83-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 389621-83-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Chemistry:
4-(Piperidine-1-carbonyl)phenylboronic acid is used as a key component in the Suzuki reaction for facilitating carbon-carbon bonding. This reaction is widely employed in the synthesis of various organic compounds, making it an essential tool in the field of organic chemistry.
Used in Pharmaceutical Industry:
4-(Piperidine-1-carbonyl)phenylboronic acid is used as a building block in the synthesis of pharmaceutical compounds. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Material Science:
4-(Piperidine-1-carbonyl)phenylboronic acid is used as a precursor in the development of new materials with specific properties, such as improved conductivity or enhanced stability. Its versatility in chemical reactions makes it a valuable asset in material science research and development.
Used in Research and Development:
4-(Piperidine-1-carbonyl)phenylboronic acid is used as a research compound for exploring new chemical reactions and understanding the underlying mechanisms. Its role in the Suzuki reaction makes it a valuable tool for advancing knowledge in the field of organic chemistry and related disciplines.

InChI:InChI=1/C12H16BNO3/c15-12(14-8-2-1-3-9-14)10-4-6-11(7-5-10)13(16)17/h4-7,16-17H,1-3,8-9H2

Downstream Products

• 1472640-87-1 (2-phenylpiperidin-1-yl)(4-(4'-(piperidine-1-carbonyl)-[1,1'-biphenyl]-4-yl)-1H-1,2,3-triazol-1-yl)methanone 
• 1542067-15-1 6-[4-(piperidine-1-carbonyl)phenyl]pyrrolo[2,3-b]pyridine-1-carboxylic acid amide 
• 1542067-49-1 piperidin-1-yl-[4-(1H-pyrrolo[2,3-b]pyridin-6-yl)phenyl]methanone 

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