254893-03-3 Usage
General Description
3-(4-Boronophenyl)cyclobutanone is a chemical compound that contains a boron atom, a phenyl group, and a cyclobutanone ring. It is a yellow crystalline solid that is commonly used as a building block in organic synthesis. 3-(4-BORONOPHENYL)CYCLOBUTANONE is known for its ability to undergo various chemical reactions, including cycloadditions and cross-coupling reactions. It has been studied for its potential applications in pharmaceutical and materials science, as well as its role in the development of new synthetic methodologies. Additionally, 3-(4-Boronophenyl)cyclobutanone has been used in the synthesis of biologically active molecules and as a versatile intermediate in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 254893-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,8,9 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 254893-03:
(8*2)+(7*5)+(6*4)+(5*8)+(4*9)+(3*3)+(2*0)+(1*3)=163
163 % 10 = 3
So 254893-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BO3/c12-10-5-8(6-10)7-1-3-9(4-2-7)11(13)14/h1-4,8,13-14H,5-6H2
254893-03-3Relevant articles and documents
4-Dihydroxyborylphenyl Analogues of 1-Aminocyclobutanecarboxylic Acids: Potential Boron Neutron Capture Therapy Agents
Srivastava, Rajiv R.,Singhaus, Robert R.,Kabalka, George W.
, p. 8495 - 8500 (2007/10/03)
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.
