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500789-07-1

BOC-(R)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID

Catalog#: AR00D8Z3  |   CAS#: 500789-07-1  |   MDL#: MFCD03427961  |   MF: C14H18BrNO4  |   MW: 344.2010

Packsize Purity Price Availability Quantity
100mg 97% $45.00 Global Stock Buy Now Add To Cart
250mg 97% $67.00 Global Stock Buy Now Add To Cart
1g 97% $163.00 Global Stock Buy Now Add To Cart
5g 97% $485.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00D8Z3
Chemical Name BOC-(R)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID
CAS Number 500789-07-1
Molecular Formula C14H18BrNO4
Molecular Weight 344.2010
MDL Number MFCD03427961
SMILES OC(=O)C[C@H](c1ccccc1Br)NC(=O)OC(C)(C)C

The (R)-3-(2-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid is a valuable compound in chemical synthesis, particularly in the field of organic chemistry. This molecule serves as a versatile building block for the preparation of various advanced organic compounds. Due to its unique structure and functional groups, it can participate in a wide range of chemical reactions, offering numerous opportunities for the design and creation of new molecules.One key application of (R)-3-(2-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid is in the synthesis of pharmaceutical intermediates. By strategically incorporating this compound into the synthesis pathways, chemists can access complex structures that are essential for the development of new drugs. The presence of both the bromophenyl group and the tert-butoxycarbonyl-protected amine moiety allows for selective modifications and functionalizations, enabling the formation of various bioactive molecules.Furthermore, this compound can be utilized in the preparation of chiral compounds due to the presence of the (R)-configuration. Chirality plays a crucial role in the biological activity of many drugs and bioactive molecules, making the synthesis of enantiopure compounds highly significant. The (R)-3-(2-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid can serve as a valuable starting material for the synthesis of chiral building blocks, enabling the creation of enantioselective products.Overall, the application of (R)-3-(2-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid in chemical synthesis offers a diverse range of possibilities for creating complex organic molecules with specific functionalities. Its unique structural features make it a valuable tool for organic chemists seeking to advance their research and develop novel compounds with potential applications in pharmaceuticals, materials science, and other fields.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H312-H332
Precautionary Statements P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class -
Packing Group -

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