105404-33-9

Basic information

• Product Name: methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate
• Synonyms: methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate;3-Quinolinecarboxylic acid,1,2,3,4-tetrahydro-2-oxo-,methyl ester;METHYL 2-OXO-1,2,3,4-TETRAHYDROQUINOLINE-3-CARBOXYLATE
• CAS NO: 105404-33-9
• Molecular Formula: C₁₁H₁₁NO₃
• Molecular Weight: 205.20994
• EINECS: -0
• Mol File: 105404-33-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate(105404-33-9)
• EPA Substance Registry System: methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate(105404-33-9)

Safety Data

• Hazardous Substances Data: 105404-33-9(Hazardous Substances Data)

Usage

General Description

Methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate is a chemical compound with the molecular formula C11H13NO3. It is a synthetic derivative of quinoline, a heterocyclic compound found in many natural products and pharmaceuticals. methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate has potential applications in medicinal chemistry and drug development due to its unique structure and reactivity. It is also used as a building block in the synthesis of various organic compounds. Methyl 1,2,3,4-tetrahydro-2-oxoquinoline-3-carboxylate is of interest to researchers and chemists for its potential biological activities and as a precursor for the synthesis of bioactive molecules.

Upstream product

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Relevant articles and documents

Ring Size and Substitution Effects in the Tandem Reduction-Lactamization of ortho-Substituted Nitroarenes

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Amine compounds, their production and use

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.