254893-07-7

Basic information

• Product Name: C₁₂H₁₃BN₂O₄
• Synonyms: C₁₂H₁₃BN₂O₄
• CAS NO: 254893-07-7
• Molecular Weight: 260.057
• Mol File: 254893-07-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₂H₁₃BN₂O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₂H₁₃BN₂O₄(254893-07-7)
• EPA Substance Registry System: C₁₂H₁₃BN₂O₄(254893-07-7)

Safety Data

• Hazardous Substances Data: 254893-07-7(Hazardous Substances Data)

Upstream product

• 151-50-8 potassium cyanide 
• 506-87-6 ammonium carbonate 
• 254893-03-3 3-(4-boronophenyl)cyclobutanone 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 254892-91-6 3-(4-bromophenyl)cyclobutanone 
• 254892-87-0 3-(4-bromophenyl)-2,2-dichlorocyclobutan-1-one 
• 254892-95-0 3-(4-bromophenyl)cyclobutanone ethylene ketal 
• 254892-99-4 3-(4-boronophenyl)cyclobutanone ethylene ketal 

Downstream Products

• 254892-82-5 1-amino-3-(4-dihydroxyborylphenyl)cyclobutanecarboxylic acid 

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.