246867-17-4 Usage
Uses
Used in Medicinal Chemistry and Drug Development:
2-OXO-1,2,3,4-TETRAHYDRO-QUINOLINE-3-CARBOXYLIC ACID is used as a building block for the synthesis of various compounds with pharmacological properties. Its unique structural features and biological activities make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Agrochemicals:
In the agrochemical industry, 2-OXO-1,2,3,4-TETRAHYDRO-QUINOLINE-3-CARBOXYLIC ACID may have potential applications as a component in the development of new pesticides, herbicides, or other agrochemical products. Its structural and biological properties could contribute to the creation of more effective and environmentally friendly solutions for agricultural challenges.
Used in Materials Science:
2-OXO-1,2,3,4-TETRAHYDRO-QUINOLINE-3-CARBOXYLIC ACID may also find applications in the field of materials science, where its unique properties could be utilized in the development of new materials with specific characteristics. This could include applications in areas such as polymers, coatings, or other advanced materials with tailored properties for various industries.
Further research and development are necessary to fully understand the potential applications and benefits of 2-OXO-1,2,3,4-TETRAHYDRO-QUINOLINE-3-CARBOXYLIC ACID in these industries and to explore additional uses that may arise from its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 246867-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,8,6 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 246867-17:
(8*2)+(7*4)+(6*6)+(5*8)+(4*6)+(3*7)+(2*1)+(1*7)=174
174 % 10 = 4
So 246867-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c12-9-7(10(13)14)5-6-3-1-2-4-8(6)11-9/h1-4,7H,5H2,(H,11,12)(H,13,14)
246867-17-4Relevant academic research and scientific papers
Amine compounds, their production and use
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, (2008/06/13)
The present invention provides a compound of the formula: wherein Ar represents an aromatic group which may be substituted; X represents methylene, S, SO, SO2or CO; Y represents a spacer having a main chain of 2 to 5 atoms; n represents an integer of 1 to 5; i) R1and R2each represents a hydrogen atom or a lower alkyl which may be substituted, ii) R1and R2form, taken together with the adjacent nitrogen atom, a nitrogen-containing heterocyclic ring which may be substituted, or iii) R1or R2together with —(CH2)n—N═ form, bonded to a component atom of Ring B, a spiro-ring which may be substituted; Ring A represents an aromatic ring which may be substituted; Ring B represents a 4- to 7-membered nitrogen-containing non-aromatic ring which may be further substituted by alkyl or acyl, with a proviso that X represents S, SO, SO2or CO when Ring A has as a substituent a group represented by the formula: —NHCOR11 where R11represents alkyl, alkoxyalkyl, alkylthioalkyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl or a group represented by the formula: —NHR12 where R12represents alkyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, or a salt thereof; which has an excellent somatostatin receptor binding inhibition action.
