(2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate
Catalog Number: BT-254371
CAS Number: 217099-43-9
Molecular Formula: C14H10N2O2S2
Molecular Weight: 302.4 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
Price:
Product Introduction
Description
(2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate, also known as CBTC, is a synthetic compound that has gained attention in recent years due to its potential therapeutic and environmental applications. CBTC belongs to the class of thiophene derivatives, which have been extensively studied for their biological and pharmacological properties.
Properties
CAS Number
217099-43-9
Product Name
(2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate
IUPAC Name
(2-carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate
Molecular Formula
C14H10N2O2S2
Molecular Weight
302.4 g/mol
InChI
InChI=1S/C14H10N2O2S2/c15-13(16)12-6-8-3-4-9(7-11(8)20-12)18-14(17)10-2-1-5-19-10/h1-7H,(H3,15,16)
InChI Key
OTGQTQBPQCRNRG-UHFFFAOYSA-N
SMILES
C1=CSC(=C1)C(=O)OC2=CC3=C(C=C2)C=C(S3)C(=N)N
Synonyms
2-amidino-6-(2-thiophene carboxy)benzothiophene methanesulfonate
BCX 1470
BCX 1470
Canonical SMILES
C1=CSC(=C1)C(=O)OC2=CC3=C(C=C2)C=C(S3)C(=N)N
Method of Synthesis or Extraction
(2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate can be synthesized using various methods, including the reaction of 2-thiophenecarboxylic acid with thiourea in the presence of a catalyst, or the reaction of 2-thiophenecarboxylic acid with cyanamide and ammonium carbonate. The efficiency and yield of each method depend on the reaction conditions, such as temperature, pressure, and reaction time. The environmental and safety considerations of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate synthesis include the use of hazardous chemicals and the generation of waste products. Therefore, it is essential to follow proper safety protocols and dispose of the waste products appropriately.
Chemical Structure and Biological Activity
The chemical structure of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate consists of a thiophene ring attached to a benzothiophene ring, with a carboxylate and carbamimidoyl group attached to the thiophene ring. (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been shown to exhibit potent antitumor activity by inhibiting the growth of cancer cells. The mechanism of action of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate involves the inhibition of tubulin polymerization, which is essential for cell division. (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has also been shown to have antibacterial and antifungal activity by disrupting the cell membrane of microorganisms.
Biological Effects
(2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been shown to have potential therapeutic effects on various diseases, including cancer, bacterial and fungal infections, and inflammation. However, (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate may also have toxic effects on normal cells and tissues, which need to be further studied. (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been shown to affect cell function and signal transduction by inhibiting the activity of enzymes and receptors involved in cell signaling pathways.
Applications
In medical research, (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been studied for its potential role in drug development, particularly in the treatment of cancer and infectious diseases. Clinical trials have shown promising results in the use of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate as a chemotherapeutic agent. However, further studies are needed to determine the safety and efficacy of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in humans. In environmental research, (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been studied for its effects on ecosystems and its potential role in pollution management. (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been shown to have low toxicity to aquatic organisms, making it a potential candidate for the treatment of contaminated water. In industrial research, (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations need to be taken into account when using (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in industrial applications.
Future Perspectives and Challenges
The current limitations in the use and study of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate include the lack of understanding of its toxicity and potential side effects. Further studies are needed to determine the safety and efficacy of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in humans and the environment. Possible solutions and improvements include the development of more efficient and environmentally friendly methods of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate synthesis and the identification of new biological targets for (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate. Future trends and prospects in the application of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in scientific research include the development of new drugs and therapies for various diseases and the use of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in environmental remediation.
Conclusion:
In conclusion, (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate is a synthetic compound with potential therapeutic and environmental applications. The methods of synthesis, chemical structure, biological activity, and potential applications of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate have been discussed in this paper. Further studies are needed to determine the safety and efficacy of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in humans and the environment. The development of more efficient and environmentally friendly methods of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate synthesis and the identification of new biological targets for (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate are essential for the future application of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in scientific research.
Conclusion:
In conclusion, (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate is a synthetic compound with potential therapeutic and environmental applications. The methods of synthesis, chemical structure, biological activity, and potential applications of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate have been discussed in this paper. Further studies are needed to determine the safety and efficacy of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in humans and the environment. The development of more efficient and environmentally friendly methods of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate synthesis and the identification of new biological targets for (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate are essential for the future application of (2-Carbamimidoyl-1-benzothiophen-6-yl) thiophene-2-carboxylate in scientific research.
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@thebiotek.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@thebiotek.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.
Category
Hot Products
2-Oxo-3-hydroxy-lysergide
CAS No.: 111295-09-1
Uricytin
CAS No.: 40919-33-3
Gadolinium (III) isopropoxide
CAS No.: 14532-05-9
5-Chloro-8-hydroxyquinoline Glucuronide
CAS No.: 65851-39-0
4,4'-Diaponeurosporene
CAS No.: 53872-50-7
Methyl 2-(4-fluorophenyl)-2-(piperidin-2-yl)acetate
CAS No.: 1354631-33-6
info@thebiotek.com
256 N Vinedo Ave, Pasadena, California 91107
