59132-30-8 Usage
General Description
2,3,4,9-Tetrahydro-1H-pyrido(3,4-b)indole-1,3-dicarboxylic acid is a complex chemical compound that is not well-known. It is a heterocyclic compound with a pyridine ring fused to an indole ring, and it contains two carboxylic acid groups. 2,3,4,9-Tetrahydro-1H-pyrido(3,4-b)indole-1,3-dicarboxylic acid is not commonly found in nature but can be synthesized in the laboratory. Its potential uses are not well-documented, but its structure suggests that it may have applications in medicinal chemistry, such as for drug development or as a molecular probe in biological research. Further studies are needed to fully understand the properties and potential uses of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 59132-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59132-30:
(7*5)+(6*9)+(5*1)+(4*3)+(3*2)+(2*3)+(1*0)=118
118 % 10 = 8
So 59132-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O4/c16-12(17)9-5-7-6-3-1-2-4-8(6)14-10(7)11(15-9)13(18)19/h1-4,9,11,14-15H,5H2,(H,16,17)(H,18,19)
59132-30-8Relevant articles and documents
Electrochemistry of Natural Products. 7. Oxidative Decarboxylation of Some Tetrahydro-β-carbolinecarboxylic Acids
Bobbitt, James M.,Willis, John P.
, p. 1978 - 1984 (2007/10/02)
A series of 1,2,3,4-tetrahydro-β-carboline-1- and -3-carboxylic acids containing various substituents in positions 1, 2, and 3 were oxidized electrochemically.In general, the acids were decarboxylated, and unsaturation was introduced into the C ring.The oxidation appears to take place through the indole ring nitrogen, and possible mechanisms of the reactions are presented.Parallels between the observed reactions and early steps in indole alkaloid biosynthesis are discussed.The oxidative dimerization of tetrahydrocarbazole is reported.
