6052-68-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4,9-TETRAHYDRO-1H-BETA-CARBOLINE-3-CARBOXYLIC ACID is used as a pharmaceutical agent for its potential therapeutic properties. The carboxy group at position 3 allows for interactions with various biological targets, making it a candidate for the development of new drugs with specific mechanisms of action.
Used in Chemical Research:
In the field of chemical research, 2,3,4,9-TETRAHYDRO-1H-BETA-CARBOLINE-3-CARBOXYLIC ACID serves as a valuable compound for studying the structure-activity relationships of beta-carbolines. Its unique substitution pattern can provide insights into the design and synthesis of novel beta-carboline-based molecules with improved pharmacological profiles.
Used in Neuroprotective Applications:
2,3,4,9-TETRAHYDRO-1H-BETA-CARBOLINE-3-CARBOXYLIC ACID is used as a neuroprotective agent due to its potential to modulate neuronal signaling pathways and protect against neurodegenerative processes. Its carboxy group may facilitate interactions with specific receptors or enzymes, contributing to its neuroprotective effects.
Check Digit Verification of cas no
The CAS Registry Mumber 6052-68-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6052-68:
(6*6)+(5*0)+(4*5)+(3*2)+(2*6)+(1*8)=82
82 % 10 = 2
So 6052-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c15-12(16)10-5-8-7-3-1-2-4-9(7)14-11(8)6-13-10/h1-4,10,13-14H,5-6H2,(H,15,16)
6052-68-2Relevant academic research and scientific papers
Some 3-carboxamides of β-carboline and tetrahydro-β-carboline
Couts, Ronald T.,Micetich, Ronald G.,Baker, Glen B,Benderly, Abraham,Dewhurst, Tim,et al.
, p. 131 - 142 (2007/10/02)
A series of tetrahydro-β-carboline-3-carboxamides (L- and D-series) was made by the interaction of the respective amine with the appriopriate methyl tetrahydro-β-carboline-3-carboxylate.The β-carboline-3-carboxamides were prepared by a similar route from methyl β-carboline-3-carboxylate or by aromatization of the respective tetrahydro-β-carboline-3-carboxamide.The diastereomers of N-sec-butyl tetrahydro-β-carboline-3-carboxamide (L- and D-series) were separated by chromatography.
