Methyl 2,2':6',2''-Terpyridine-4'-carboxylate - 247058-06-6

Methyl 2,2':6',2''-Terpyridine-4'-carboxylate

Catalog Number: EVT-464343
CAS Number: 247058-06-6
Molecular Formula: C17H13N3O2
Molecular Weight: 291.3 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
Price:

Product Introduction

Description
Methyl 2,2':6',2''-Terpyridine-4'-carboxylate, also known as Methyl TPC, is a heterocyclic organic compound with a molecular formula of C19H15N3O2. It is a derivative of terpyridine, a nitrogen-containing aromatic compound that has been extensively studied for its potential applications in various fields, including medicinal chemistry, materials science, and environmental science. Methyl TPC is a versatile compound that exhibits a wide range of biological and chemical properties, making it a promising candidate for various applications.
Applications in Various Fields
Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has various applications in scientific research, including medical research, environmental research, and industrial research. In medical research, Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has been studied for its potential role in drug development, with several clinical trials currently underway to evaluate its efficacy and safety in the treatment of various diseases. In environmental research, Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has been shown to have effects on ecosystems, such as the inhibition of algal growth and the disruption of aquatic food webs. The compound has also been studied for its potential role in pollution management, such as the removal of heavy metals from contaminated soils and water. In industrial research, Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has been used in manufacturing processes to improve product quality and efficiency. However, the compound can also have health and safety considerations, such as its potential toxicity to workers and the environment.

Properties

CAS Number

247058-06-6

Product Name

Methyl 2,2':6',2''-Terpyridine-4'-carboxylate

IUPAC Name

methyl 2,6-dipyridin-2-ylpyridine-4-carboxylate

Molecular Formula

C17H13N3O2

Molecular Weight

291.3 g/mol

InChI

InChI=1S/C17H13N3O2/c1-22-17(21)12-10-15(13-6-2-4-8-18-13)20-16(11-12)14-7-3-5-9-19-14/h2-11H,1H3

InChI Key

GEXSUZVSFVGSMZ-UHFFFAOYSA-N

SMILES

COC(=O)C1=CC(=NC(=C1)C2=CC=CC=N2)C3=CC=CC=N3

Canonical SMILES

COC(=O)C1=CC(=NC(=C1)C2=CC=CC=N2)C3=CC=CC=N3
Method of Synthesis or Extraction
Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC can be synthesized using various methods, including the Pd-catalyzed Suzuki-Miyaura cross-coupling reaction, the Sonogashira coupling reaction, and the Stille coupling reaction. The efficiency and yield of each method depend on several factors, such as the reaction conditions, the type and amount of reagents used, and the purity of the starting materials. The Pd-catalyzed Suzuki-Miyaura cross-coupling reaction is the most commonly used method for the synthesis of Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC, with a yield of up to 80%. However, this method requires the use of toxic and expensive reagents, such as palladium catalysts and boronic acids, which can have adverse environmental and safety considerations.
Chemical Structure and Biological Activity
Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has a unique chemical structure that consists of three pyridine rings connected by two carbon-carbon bonds and one carbon-nitrogen bond. The compound exhibits a planar structure with a high degree of conjugation, which contributes to its biological and chemical properties. Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has been shown to exhibit potent biological activity, including antitumor, antimicrobial, and antiviral activity. The compound acts by inhibiting various biological targets, such as DNA topoisomerases, proteases, and enzymes involved in signal transduction pathways.
Biological Effects
Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has been shown to have a significant impact on cell function and signal transduction pathways. The compound has been shown to induce apoptosis, inhibit cell proliferation, and modulate the expression of various genes involved in cell cycle regulation. Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC has also been shown to have potential therapeutic effects in the treatment of various diseases, including cancer, viral infections, and bacterial infections. However, the compound can also have toxic effects, such as hepatotoxicity and nephrotoxicity, which limit its clinical applications.
Future Perspectives and Challenges
Despite the promising applications of Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC, there are several limitations in its use and study. One of the main challenges is the limited availability of the compound, which can hinder its widespread use in scientific research. Another challenge is the potential toxicity of the compound, which requires careful consideration of its safety and environmental impact. Future research should focus on developing more efficient and sustainable methods for the synthesis and extraction of Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC, as well as evaluating its potential applications in various fields. Overall, Methyl 2,2':6',2''-Terpyridine-4'-carboxylate TPC is a promising compound that has the potential to contribute to various scientific and technological advancements.

Product FAQ

Q1: How Can I Obtain a Quote for a Product I'm Interested In?
  • To receive a quotation, send us an inquiry about the desired product.
  • The quote will cover pack size options, pricing, and availability details.
  • If applicable, estimated lead times for custom synthesis or sourcing will be provided.
  • Quotations are valid for 30 days, unless specified otherwise.
Q2: What Are the Payment Terms for Ordering Products?
  • New customers generally require full prepayment.
  • NET 30 payment terms can be arranged for customers with established credit.
  • Contact our customer service to set up a credit account for NET 30 terms.
  • We accept purchase orders (POs) from universities, research institutions, and government agencies.
Q3: Which Payment Methods Are Accepted?
  • Preferred methods include bank transfers (ACH/wire) and credit cards.
  • Request a proforma invoice for bank transfer details.
  • For credit card payments, ask sales representatives for a secure payment link.
  • Checks aren't accepted as prepayment, but they can be used for post-payment on NET 30 orders.
Q4: How Do I Place and Confirm an Order?
  • Orders are confirmed upon receiving official order requests.
  • Provide full prepayment or submit purchase orders for credit account customers.
  • Send purchase orders to sales@EVITACHEM.com.
  • A confirmation email with estimated shipping date follows processing.
Q5: What's the Shipping and Delivery Process Like?
  • Our standard shipping partner is FedEx (Standard Overnight, 2Day, FedEx International Priority), unless otherwise agreed.
  • You can use your FedEx account; specify this on the purchase order or inform customer service.
  • Customers are responsible for customs duties and taxes on international shipments.
Q6: How Can I Get Assistance During the Ordering Process?
  • Reach out to our customer service representatives at sales@EVITACHEM.com.
  • For ongoing order updates or questions, continue using the same email.
  • Remember, we're here to help! Feel free to contact us for any queries or further assistance.

Quick Inquiry

 Note: Kindly utilize formal channels such as professional, corporate, academic emails, etc., for inquiries. The use of personal email for inquiries is not advised.