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39161-84-7

2-(4-Mercaptophenyl)acetic acid

Catalog#: AR003MAY  |   CAS#: 39161-84-7  |   MDL#: MFCD00797617  |   MF: C8H8O2S  |   MW: 168.2129

Packsize Purity Price Availability Quantity
100mg 96% $5.00 Global Stock Buy Now Add To Cart
250mg 96% $9.00 Global Stock Buy Now Add To Cart
1g 96% $28.00 Global Stock Buy Now Add To Cart
5g 96% $79.00 Global Stock Buy Now Add To Cart
25g 96% $380.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003MAY
Chemical Name 2-(4-Mercaptophenyl)acetic acid
CAS Number 39161-84-7
Molecular Formula C8H8O2S
Molecular Weight 168.2129
MDL Number MFCD00797617
SMILES OC(=O)Cc1ccc(cc1)S

2-(4-Mercaptophenyl)acetic acid, also known as MPAA, is a versatile chemical compound frequently employed in chemical synthesis as a key intermediate. Its unique structure containing a mercapto group and a phenyl ring allows for various reactions and transformations, making it a valuable building block in organic synthesis.One of the primary applications of 2-(4-Mercaptophenyl)acetic acid is in the synthesis of thiol-containing compounds. The mercapto group in MPAA serves as a reactive site for thiol-ene or thiol-alkene reactions, enabling the introduction of sulfur-containing functionalities into target molecules. This is particularly useful in the modification of biomolecules, polymers, and materials for various applications in pharmaceuticals, materials science, and chemical biology.Additionally, 2-(4-Mercaptophenyl)acetic acid can be utilized in the synthesis of conjugated molecules and polymers. By linking MPAA to suitable precursors through its carboxylic acid group, researchers can create conjugated systems with enhanced electronic properties. These materials find applications in organic electronics, optoelectronics, and sensor technologies due to their tunable optical and electronic characteristics.Furthermore, the reactivity of 2-(4-Mercaptophenyl)acetic acid can be harnessed in the preparation of surface-functionalized materials. Coupling reactions involving MPAA can be used to anchor the compound onto surfaces or nanoparticles, imparting desired chemical properties such as improved adhesion, wettability, or catalytic activity. This strategy is commonly employed in surface modification for sensor development, catalysis, and bioconjugation purposes.Overall, 2-(4-Mercaptophenyl)acetic acid serves as a valuable tool in chemical synthesis, offering a wide range of opportunities for the construction of complex molecules, functional materials, and tailored surfaces with diverse applications in research and industry.
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GHS Pictogram
Signal Word Danger
UN# 3335
Hazard Statements H315-H318-H335
Precautionary Statements P261-P280-P305+P351+P338
Class 9
Packing Group

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