naphthalen-2-yl (2S)-3-phenyl-2-(phenylformamido)propanoate

Base Information

• Chemical Name: naphthalen-2-yl (2S)-3-phenyl-2-(phenylformamido)propanoate
• CAS No.: 15873-25-3
• Molecular Formula: C26H21 N O3
• Molecular Weight: 395.44984
• DSSTox Substance ID: DTXSID601248299
• Nikkaji Number: J231.989F
• Mol file: 15873-25-3.mol

Synonyms:L-Phenylalanine, N-benzoyl-, 2-naphthalenyl ester;SCHEMBL11329819;DTXSID601248299;naphthalen-2-yl (2S)-3-phenyl-2-(phenylformamido)propanoate;AKOS037646313;N-Benzoylphenylalanine 2-naphthyl ester;benzoyl-3-phenylalanine 2-naphthyl ester;AS-68081;D95265;N-Benzoyl-L-phenylalanine 2-naphthalenyl ester

Chemical Property of naphthalen-2-yl (2S)-3-phenyl-2-(phenylformamido)propanoate

Chemical Property:

• Vapor Pressure: 4.1E-17mmHg at 25°C
• Melting Point: 158 °C
• Refractive Index: 1.648
• Boiling Point: 656.6oC at 760 mmHg
• Flash Point: 350.9oC
• PSA: 55.40000
• Density: 1.222g/cm3
• LogP: 5.17740
• Solubility.: almost transparency in hot Methanol
• XLogP3: 5.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 395.15214353
• Heavy Atom Count: 30
• Complexity: 565

Purity/Quality:

98%,99%, ^*data from raw suppliers

N-Benzoyl-DL-phenylalanine2-NaphthylEster ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CC(C(=O)OC2=CC3=CC=CC=C3C=C2)NC(=O)C4=CC=CC=C4
• Isomeric SMILES: C1=CC=C(C=C1)C[C@@H](C(=O)OC2=CC3=CC=CC=C3C=C2)NC(=O)C4=CC=CC=C4

Technology Process of naphthalen-2-yl (2S)-3-phenyl-2-(phenylformamido)propanoate

There total 1 articles about naphthalen-2-yl (2S)-3-phenyl-2-(phenylformamido)propanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N-benzoyl-DL-phenylalanine β-naphthyl ester (2134-24-9) → N-benzoyl-L-phenylalanine β-naphthyl ester (15873-25-3) + N-benzoyl-D-phenylalanine β-naphthyl ester (211681-82-2)

Guidance literature:

With N-[(S)-1-phenylethyl]carbamoyl-derivatized cyclofructan-6 column; In ethanol; n-heptane; trifluoroacetic acid; at 20 ℃; Resolution of racemate;

DOI:10.1021/ac902257a

upstream raw materials:

N-benzoyl-DL-phenylalanine β-naphthyl ester