Cas no 16367-71-8 (tert-Butyl 2-Amino-3-phenylpropanoate)

Tert-Butyl 2-Amino-3-phenylpropanoate is a chiral amino acid ester derivative widely used as a key intermediate in organic synthesis and pharmaceutical applications. Its tert-butyl ester group enhances solubility in organic solvents while providing steric protection for the amine functionality, making it valuable for peptide coupling and asymmetric synthesis. The phenylpropanoate backbone offers versatility for further functionalization, enabling the synthesis of bioactive compounds. This compound is particularly useful in medicinal chemistry for the development of peptidomimetics and small-molecule inhibitors. High purity grades ensure consistent performance in sensitive reactions, while its stability under standard storage conditions makes it a reliable reagent for research and industrial processes.
tert-Butyl 2-Amino-3-phenylpropanoate structure
16367-71-8 structure
Product Name:tert-Butyl 2-Amino-3-phenylpropanoate
CAS No:16367-71-8
MF:C13H19NO2
MW:221.29546380043
CID:1347717
PubChem ID:262751
Update Time:2025-10-28

tert-Butyl 2-Amino-3-phenylpropanoate Chemical and Physical Properties

Names and Identifiers

    • Phenylalanine, 1,1-dimethylethyl ester
    • D-Phenylalanine 1.1-Dimethylethyl ester
    • tert-butyl 2-amino-3-phenylpropanoate
    • DTXSID301347222
    • 16367-71-8
    • SCHEMBL1221379
    • MFCD12762205
    • EN300-113093
    • l-phe t-butyl ester
    • AM20030026
    • G71311
    • tert-butyl2-amino-3-phenylpropanoate
    • Z600614494
    • D,L-phenylalanine tert-butyl ester
    • 2-Amino-3-phenyl-propionic acid tert-butyl ester
    • AKOS009156747
    • DB-352839
    • QOISWWBTZMFUEL-UHFFFAOYSA-N
    • tert-Butyl 2-Amino-3-phenylpropanoate
    • Inchi: 1S/C13H19NO2/c1-13(2,3)16-12(15)11(14)9-10-7-5-4-6-8-10/h4-8,11H,9,14H2,1-3H3
    • InChI Key: QOISWWBTZMFUEL-UHFFFAOYSA-N
    • SMILES: O(C(C(CC1C=CC=CC=1)N)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 221.14167
  • Monoisotopic Mass: 221.142
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 5
  • Complexity: 227
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.1
  • Topological Polar Surface Area: 52.3?2

Experimental Properties

  • PSA: 52.32

tert-Butyl 2-Amino-3-phenylpropanoate Pricemore >>

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Additional information on tert-Butyl 2-Amino-3-phenylpropanoate

Exploring tert-Butyl 2-Amino-3-phenylpropanoate (CAS No. 16367-71-8): Properties, Applications, and Market Insights

tert-Butyl 2-Amino-3-phenylpropanoate (CAS No. 16367-71-8) is a specialized organic compound widely recognized in the pharmaceutical and chemical industries. This ester derivative of phenylalanine features a tert-butyl group, which enhances its stability and solubility, making it a valuable intermediate in synthetic chemistry. Researchers and manufacturers frequently seek this compound for its role in peptide synthesis, drug development, and chiral building blocks.

The growing interest in tert-Butyl 2-Amino-3-phenylpropanoate is driven by its versatility in medicinal chemistry. With the rise of personalized medicine and biopharmaceuticals, this compound has gained attention for its potential in designing enzyme inhibitors and receptor modulators. Its CAS No. 16367-71-8 is often searched in academic databases and chemical catalogs, reflecting its relevance in cutting-edge research.

From a structural perspective, tert-Butyl 2-Amino-3-phenylpropanoate combines a phenyl group with an amino acid backbone, offering unique reactivity. This makes it ideal for asymmetric synthesis and catalysis, particularly in the production of optically active compounds. The tert-butyl ester moiety further provides steric protection, improving yield in multi-step reactions.

In the context of green chemistry, tert-Butyl 2-Amino-3-phenylpropanoate aligns with the demand for sustainable synthetic routes. Researchers are exploring its use in microwave-assisted reactions and flow chemistry, reducing solvent waste and energy consumption. These innovations address the increasing focus on environmentally friendly processes in the chemical industry.

The market for tert-Butyl 2-Amino-3-phenylpropanoate is expanding, particularly in regions with strong pharmaceutical R&D sectors. Suppliers often highlight its high purity grades (e.g., >98%) to meet the stringent requirements of GMP manufacturing. Additionally, its CAS No. 16367-71-8 is frequently cross-referenced with custom synthesis services, catering to niche applications.

For laboratories handling tert-Butyl 2-Amino-3-phenylpropanoate, proper storage conditions (e.g., dry, cool environments) are critical to maintain its stability. Analytical techniques like HPLC and NMR are commonly employed to verify its identity and purity, ensuring compliance with research protocols and industrial standards.

Looking ahead, the demand for tert-Butyl 2-Amino-3-phenylpropanoate is expected to grow alongside advancements in peptide-based therapeutics and small-molecule drugs. Its CAS No. 16367-71-8 will remain a key identifier in scientific literature and procurement systems, reinforcing its status as a cornerstone in modern synthetic chemistry.

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