Product Name:(R)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid

IUPAC Name:(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(4-tert-butylphenyl)propanoic acid

CAS:250611-12-2
Molecular Formula:C18H27NO4
Purity:95%
Catalog Number:CM192167
Molecular Weight:321.42

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CM192167-10g 3-4 Weeks ŁĜǟ

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Product Details

CAS NO:250611-12-2
Molecular Formula:C18H27NO4
Melting Point:-
Smiles Code:O=C(O)[C@H](NC(OC(C)(C)C)=O)CC1=CC=C(C(C)(C)C)C=C1
Density:
Catalog Number:CM192167
Molecular Weight:321.42
Boiling Point:461.413°C at 760 mmHg
MDL No:MFCD02094579
Storage:Store at 2-8°C.

Category Infos

Amino Acids and Peptides
Amino acids are organic compounds containing a basic amino group and an acidic carboxyl group. Because amino acids contain both amino and carboxyl groups, they can be polymerized in an end-to-end manner, removing a molecule of water to form a covalent amide bond or peptide bond. Many amino acids are linked together end to end to form a polypeptide. Amino acids and peptides are important components in the fields of medicine and life sciences.
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Product Other Information

Product Overview (R)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid is an organic compound that has been used in a variety of scientific research applications. This compound is a chiral carboxylic acid that is synthesized through a multi-step process and has a variety of biochemical and physiological effects.
Chemical Properties (R)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid is a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes.
Synthesis and Application (R)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid has been used in a variety of scientific research applications. It has been used as a chiral auxiliary in the enantioselective synthesis of carboxylic acids, as a chiral ligand in asymmetric catalysis, and as a chiral additive in the synthesis of chiral polymers. It has also been used as a chiral building block in the synthesis of drugs, as a reagent in the synthesis of polyesters and polyamides, and as a reagent in the synthesis of polysaccharides.
Storage and Handling Sealed in dry at 2-8°C.