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Catalog No. RY084114CAS 50741-46-3

Ethyl quinoline-3-carboxylate

In Stock
Purity95%
Categoryheterocyclic

Molecular Structure

Ethyl quinoline-3-carboxylate chemical structure (CAS 50741-46-3)
Source: PubChem

Pricing & Availability

Pack SizePriceAvailability
100mg$10.00In StockInquire
250mg$13.00In StockInquire
1g$25.00In StockInquire
5g$77.00In StockInquire
25g$360.00In StockInquire

Total stock: 50g • Ships within 1-2 business days

Specifications

Catalog No.RY084114
CAS No.50741-46-3
Molecular Formula-
Molecular Weight-
Purity95%
SMILESO=C(C1=CC2=CC=CC=C2N=C1)OCC
MDL NumberMFCD00957421
Categoryheterocyclic
AvailabilityIn Stock

Synonyms & Alternative Names

Ethyl quinoline-3-carboxylate (IUPAC)Raynchem RY084114

Product Description

Ethyl quinoline-3-carboxylate (CAS 50741-46-3) is a high-quality chemical intermediate offered by Raynchem for pharmaceutical, agrochemical, and material science research. The SMILES notation for Ethyl quinoline-3-carboxylate is O=C(C1=CC2=CC=CC=C2N=C1)OCC, representing its complete molecular connectivity for computational chemistry and cheminformatics applications. Our Ethyl quinoline-3-carboxylate is available with a guaranteed purity of 95%, ensuring consistent and reliable results for your R&D and production needs. Each batch is accompanied by a Certificate of Analysis (COA) verifying identity, purity, and quality. Raynchem provides worldwide fast shipping, competitive pricing, and comprehensive technical support. COA and SDS documents are available upon request. Contact us today for bulk quantities and custom synthesis inquiries.

Applications

  • ●Pharmaceutical Intermediate Synthesis: Ethyl quinoline-3-carboxylate (CAS 50741-46-3) serves as a versatile building block in the synthesis of active pharmaceutical ingredients (APIs), enabling the construction of complex molecular architectures through palladium-catalyzed cross-coupling reactions such as Suzuki, Buchwald-Hartwig, and Heck reactions.
  • ●Agrochemical Development: This compound is utilized in the preparation of novel agrochemical agents, including herbicides, insecticides, and fungicides, where its halogenated aromatic structure provides key reactivity for further functionalization.
  • ●Material Science Research: Ethyl quinoline-3-carboxylate is employed in the development of organic electronic materials, coordination polymers, and functional dyes, where its aromatic amine moiety contributes to optoelectronic properties.
  • ●Fine Chemical Manufacturing: Ethyl quinoline-3-carboxylate is suitable for scale-up from milligram to kilogram quantities, supporting both early-stage discovery and late-stage production needs.

Safety & Handling

Hazard Information

  • !Ethyl quinoline-3-carboxylate may cause mild irritation to skin, eyes, and respiratory tract.
  • !Handle with standard laboratory precautions.
  • !Contains nitrogen — handle as a potential irritant and avoid formation of nitrogen oxides.

Precautionary Measures

  • ✓Wear appropriate personal protective equipment (PPE): chemical-resistant gloves, safety goggles, and laboratory coat.
  • ✓Work in a well-ventilated fume hood when handling Ethyl quinoline-3-carboxylate.
  • ✓Avoid direct contact with skin, eyes, and clothing. Do not breathe dust, vapors, or aerosols.
  • ✓Wash hands thoroughly after handling. Remove contaminated clothing before reuse.

This information is provided as a general guide. Always consult the Safety Data Sheet (SDS) for complete safety information before handling.

Storage & Stability

  • ●Ethyl quinoline-3-carboxylate should be stored in a cool, dry place away from direct sunlight and moisture.
  • ●Keep the container tightly sealed when not in use to prevent degradation and contamination.
  • ●Store separately from incompatible materials such as strong oxidizing agents, acids, and bases.
  • ●Under proper storage conditions, the shelf life of this product is typically 24 months from the date of manufacture.

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