Understanding the Chemical Properties of 2-(4-Bromothiophen-2-yl)acetic Acid
For chemists and product formulators, a deep understanding of a chemical compound's properties is fundamental to its successful application. 2-(4-Bromothiophen-2-yl)acetic Acid (CAS: 161942-89-8) is a prime example of a versatile intermediate whose utility is defined by its unique chemical characteristics. Whether you are looking to buy 2-(4-bromothiophen-2-yl)acetic acid for synthesis or research, knowing these properties is essential.
Molecular Structure and Identity
The chemical identity of 2-(4-Bromothiophen-2-yl)acetic Acid is encapsulated by its molecular formula, C6H5BrO2S, and its specific CAS Registry Number, 161942-89-8. Structurally, it features a thiophene ring, a five-membered heterocyclic aromatic ring containing sulfur. This ring is substituted at the 4-position with a bromine atom and at the 2-position with an acetic acid group (-CH2COOH). This arrangement provides distinct reactive sites: the bromine atom is amenable to various coupling reactions (like palladium-catalyzed cross-couplings), while the carboxylic acid group can undergo esterification, amidation, or salt formation.
Key Physical and Chemical Properties
Understanding the physical properties of 2-(4-Bromothiophen-2-yl)acetic Acid is vital for handling and processing:
- Appearance: It is typically described as a white solid, making it convenient for weighing and manipulation in laboratory settings.
- Melting Point: A critical indicator of purity, its melting point is reported in the range of 87-92°C. Variations outside this range might suggest the presence of impurities.
- Solubility: While specific solubility data may vary, such organic acids are generally soluble in common organic solvents like ethanol, methanol, and DMSO, and may have limited solubility in water.
- Reactivity: The presence of the bromine atom makes it an excellent substrate for electrophilic aromatic substitution and transition metal-catalyzed cross-coupling reactions. The acidic proton of the carboxylic acid group can be readily removed by bases.
Sourcing High-Quality Intermediates
For researchers and manufacturers, sourcing this compound requires attention to detail. A reliable 2-(4-bromothiophen-2-yl)acetic acid supplier China-based, such as NINGBO INNO PHARMCHEM CO.,LTD., is crucial. They can provide detailed specifications, ensuring the chemical meets the required purity and characteristics. Enquiring about CAS 161942-89-8 prices and requesting a Certificate of Analysis (CoA) are standard practices when evaluating a 2-(4-bromothiophen-2-yl)acetic acid manufacturer.
In summary, the chemical properties of 2-(4-Bromothiophen-2-yl)acetic Acid, including its molecular structure, functional groups, and physical attributes, dictate its broad utility in synthesis. By partnering with knowledgeable suppliers, chemists can ensure they acquire high-quality intermediates for their critical research and development projects.
Perspectives & Insights
Nano Explorer 01
"Melting Point: A critical indicator of purity, its melting point is reported in the range of 87-92°C."
Data Catalyst One
"Solubility: While specific solubility data may vary, such organic acids are generally soluble in common organic solvents like ethanol, methanol, and DMSO, and may have limited solubility in water."
Chem Thinker Labs
"Reactivity: The presence of the bromine atom makes it an excellent substrate for electrophilic aromatic substitution and transition metal-catalyzed cross-coupling reactions."