Exploring the Chemical Properties and Uses of L-2-(3-Thienyl)glycine
In the dynamic landscape of chemical manufacturing and scientific research, specific compounds emerge as indispensable tools. L-2-(3-Thienyl)glycine, identifiable by its CAS number 1194-87-2, is one such molecule. Its unique chemical profile and broad applicability make it a compound of significant interest to chemists, researchers, and product formulators. As a dedicated manufacturer and supplier, we aim to provide clarity on this important fine chemical intermediate.
The Chemical Identity of L-2-(3-Thienyl)glycine
L-2-(3-Thienyl)glycine is an alpha-amino acid derivative. Its structure is notable for the presence of a thiophene ring, a sulfur-containing aromatic heterocycle, linked to the chiral alpha-carbon of glycine. This specific arrangement confers unique reactivity and properties, distinguishing it from simpler amino acids. Typically supplied as a white to off-white solid or powder, its purity levels are critical for its intended applications, with specifications commonly exceeding 97%.
Key Chemical Properties and Characteristics
The chemical properties of L-2-(3-Thienyl)glycine are central to its utility:
- Chirality: As an L-amino acid, it possesses a specific stereochemistry, crucial for applications where stereoselectivity is paramount, particularly in pharmaceutical synthesis.
- Thiophene Moiety: The thiophene ring introduces aromaticity and sulfur heteroatom, influencing its electronic properties and potential interactions in chemical reactions.
- Amphoteric Nature: Like other amino acids, it exhibits amphoteric behavior, capable of acting as both an acid and a base.
- Solubility: Information on its solubility in various solvents is essential for reaction design and purification processes. It is generally described as sparingly soluble in water.
Applications Driving Demand and Purchase Decisions
The versatility of L-2-(3-Thienyl)glycine is evident in its diverse applications:
- Building Block in Organic Synthesis: It serves as a fundamental building block for creating more complex organic molecules. Chemists seeking to buy this compound often do so for the construction of specialized heterocycles and fine chemicals.
- Precursor for Specialty Chemicals: It is utilized as a precursor in the synthesis of other thiophenyl derivatives and compounds with tailored functionalities.
- Research and Development: In academic and industrial labs, it is a key reagent for exploring new synthetic methodologies, developing novel materials, and advancing biochemical understanding, especially in areas like proteomics.
Securing Your Supply of L-2-(3-Thienyl)glycine
For research scientists and chemical purchasers, sourcing L-2-(3-Thienyl)glycine from a reliable manufacturer is key. When inquiring about price or availability, it's important to confirm the CAS number (1194-87-2) and the specified purity. As a supplier, we focus on providing consistent quality to meet the demanding requirements of our clients. Whether you need small research quantities or bulk industrial supply, understanding the product's specifications and the supplier's capabilities is essential.
In conclusion, L-2-(3-Thienyl)glycine is a valuable and versatile compound. Its specific chemical properties, combined with its utility in synthesis and research, make it a sought-after ingredient. As a leading manufacturer and supplier, we are committed to providing high-quality L-2-(3-Thienyl)glycine to support your innovative projects and production needs.
Perspectives & Insights
Core Pioneer 24
“Solubility: Information on its solubility in various solvents is essential for reaction design and purification processes.”
Silicon Explorer X
“Applications Driving Demand and Purchase Decisions The versatility of L-2-(3-Thienyl)glycine is evident in its diverse applications: Building Block in Organic Synthesis: It serves as a fundamental building block for creating more complex organic molecules.”
Quantum Catalyst AI
“Chemists seeking to buy this compound often do so for the construction of specialized heterocycles and fine chemicals.”