(S)-2-Amino-5-(naphthalen-2-ylamino)-5-oxopentanoic acid

Base Information

• Chemical Name: (S)-2-Amino-5-(naphthalen-2-ylamino)-5-oxopentanoic acid
• CAS No.: 14525-44-1
• Molecular Formula: C₁₅H₁₆N₂O₃
• Molecular Weight: 272.304
• Hs Code.: 2924299090
• European Community (EC) Number: 238-542-7
• Wikidata: Q27162551
• ChEMBL ID: CHEMBL4069702
• Mol file: 14525-44-1.mol

Synonyms:14525-44-1;(S)-2-Amino-5-(naphthalen-2-ylamino)-5-oxopentanoic acid;L-Glutamic acid gamma-(beta-naphthylamide);H-Glu(betaNA)-OH;N-(gamma-L-glutamyl)-2-naphthylamine;N-(2-naphthyl)-L-glutamine;N-(beta-naphthyl)-L-glutamine;N-naphthalen-2-yl-L-glutamine;L-Glutamine,N-2-naphthalenyl-;CHEMBL4069702;SCHEMBL10908490;CHEBI:90444;MFCD00037743;L-glutamic acid gamma-2-naphthylamide;FD21469;AS-49083;A884637;Q27162551

Chemical Property of (S)-2-Amino-5-(naphthalen-2-ylamino)-5-oxopentanoic acid

Chemical Property:

• Vapor Pressure: 1.01E-14mmHg at 25°C
• Refractive Index: 1.679
• Boiling Point: 649.1 °C at 760 mmHg
• PKA: 2.22±0.10(Predicted)
• Flash Point: 346.4 °C
• PSA: 92.42000
• Density: 1.329 g/cm³
• LogP: 2.74370
• Storage Temp.: 2-8°C
• XLogP3: -1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 272.11609238
• Heavy Atom Count: 20
• Complexity: 359

Purity/Quality:

97% ^*data from raw suppliers

L-Glutamic acid γ-(β-naphthylamide) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 40
• Safety Statements: 22-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC=C2C=C(C=CC2=C1)NC(=O)CCC(C(=O)O)N
• Isomeric SMILES: C1=CC=C2C=C(C=CC2=C1)NC(=O)CC[C@@H](C(=O)O)N
• Uses: L-Glutamic acid gamma-(beta-naphthylamide)

Technology Process of (S)-2-Amino-5-(naphthalen-2-ylamino)-5-oxopentanoic acid

There total 1 articles about (S)-2-Amino-5-(naphthalen-2-ylamino)-5-oxopentanoic acid 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-phthalyl-L-glutamic anhydride (25830-77-7,3085-92-5) + naphthalen-2-ylamine (91-59-8) → 2-Amino-4-(naphthalen-2-ylcarbamoyl)-butyric acid (6367-24-4,14525-44-1,140851-02-1)

Guidance literature:

In 1,4-dioxane; at 40 ℃; Product distribution; other time;

DOI:10.1021/ac00278a059

upstream raw materials:

N-phthalyl-L-glutamic anhydride

naphthalen-2-ylamine