72471-59-1 Usage
Uses
Used in Pharmaceutical Industry:
2-Succinylbenzoyl-coenzyme A is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly those involved in the production of antibiotics and other therapeutic agents. Its unique structure allows it to participate in key reactions, facilitating the formation of essential drugs.
Used in Biochemical Research:
In the field of biochemistry, 2-succinylbenzoyl-coenzyme A is utilized as a research tool to study the mechanisms of enzyme-catalyzed reactions and the role of coenzyme A in cellular metabolism. This helps researchers gain a deeper understanding of various biological processes and develop targeted therapies for specific diseases.
Used in Industrial Biocatalysis:
2-Succinylbenzoyl-coenzyme A is employed in industrial biocatalysis as a substrate or cofactor for enzymes involved in the production of specialty chemicals, such as flavors, fragrances, and other high-value compounds. Its ability to participate in various enzymatic reactions makes it a valuable asset in the development of sustainable and efficient bioprocesses.
Used in Drug Delivery Systems:
Similar to gallotannin, 2-succinylbenzoyl-coenzyme A can also be incorporated into drug delivery systems to enhance the bioavailability and therapeutic efficacy of certain pharmaceutical agents. Its unique properties allow it to be used as a carrier or enhancer for targeted drug delivery, potentially improving the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 72471-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,7 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72471-59:
(7*7)+(6*2)+(5*4)+(4*7)+(3*1)+(2*5)+(1*9)=131
131 % 10 = 1
So 72471-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C32H44N7O20P3S/c1-32(2,26(45)29(46)35-10-9-21(41)34-11-12-63-31(47)18-6-4-3-5-17(18)19(40)7-8-22(42)43)14-56-62(53,54)59-61(51,52)55-13-20-25(58-60(48,49)50)24(44)30(57-20)39-16-38-23-27(33)36-15-37-28(23)39/h3-6,15-16,20,24-26,30,44-45H,7-14H2,1-2H3,(H,34,41)(H,35,46)(H,42,43)(H,51,52)(H,53,54)(H2,33,36,37)(H2,48,49,50)/t20-,24-,25-,26+,30-/m1/s1
72471-59-1Relevant academic research and scientific papers
SYNTHESIS AND REVISED STRUCTURE OF THE O-SUCCINYLBENZOIC ACID COENZYME A ESTER, AN INTERMEDIATE IN MENAQUINONE BIOSYNTHESIS
Kolkmann, R.,Leistner, E.
, p. 1703 - 1704 (2007/10/02)
Synthesis of the two isomers 2, 3 of the mono coenzyme A ester of o-succinylbenzoic acid (1, OSB, i.e. 4-(2-carboxyphenyl)-4-oxobutanoic acid) and enzymic conversion of 3 to 1,4-dihydroxy-2-naphtoic acid 7 shows that as opposed to previous assumptions the "aliphatic" rather than the"aromatic" carboxyl group in o-succinylbenzoic acid 1 is activated during vitamin K2 biosynthesis in Escherichia coli and Myobacterium phlei.
