(R)-2-Amino-3-(1H-imidazol-1-YL)propanoic acid

Base Information

• Chemical Name: (R)-2-Amino-3-(1H-imidazol-1-YL)propanoic acid
• CAS No.: 848396-10-1
• Molecular Formula: C₆H₉N₃O₂
• Molecular Weight: 155.156
• Hs Code.: 2933290090
• DSSTox Substance ID: DTXSID10704901
• Nikkaji Number: J609.678F
• Mol file: 848396-10-1.mol

Synonyms:848396-10-1;(R)-2-AMINO-3-(1H-IMIDAZOL-1-YL)PROPANOIC ACID;beta-Imidazolyl-D-Ala;3-(1H-Imidazol-1-yl)-D-alanine;(2R)-2-amino-3-imidazol-1-ylpropanoic acid;(R)-2-Amino-3-(imidazol-1-yl)propanoic acid;DTXSID10704901;MFCD08063263;AKOS016843875;AC-4465;(R)-2-AMINO-3-(1H-IMIDAZOL-1-YL)PROPANOICACID;D-Imidazolylalanine, (R)-2-Amino-3-(1H-imidazol-1-yl)propanoic acid

Chemical Property of (R)-2-Amino-3-(1H-imidazol-1-YL)propanoic acid

Chemical Property:

• Vapor Pressure: 1.04E-07mmHg at 25°C
• Refractive Index: 1.631
• Boiling Point: 417.3 °C at 760 mmHg
• Flash Point: 206.2 °C
• PSA: 95.58000
• Density: 1.44g/cm3
• LogP: -0.92860
• Storage Temp.: 2-8°C
• XLogP3: -3.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 155.069476538
• Heavy Atom Count: 11
• Complexity: 151

Purity/Quality:

99.3% ^*data from raw suppliers

(R)-2-Amino-3-(1H-imidazol-1-yl)propanoicacid 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CN(C=N1)CC(C(=O)O)N
• Isomeric SMILES: C1=CN(C=N1)C[C@H](C(=O)O)N

Technology Process of (R)-2-Amino-3-(1H-imidazol-1-YL)propanoic acid

There total 1 articles about (R)-2-Amino-3-(1H-imidazol-1-YL)propanoic 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:

1H-imidazole (288-32-4) → (S)-2-amino-3-(1H-imidazol-1-yl)propionic acid (114717-14-5,68068-70-2) + (R)-2-amino-3-(imidazol-1-yl)propanoic acid (848396-10-1,68068-70-2)

Guidance literature:

With hydrogenchloride; potassium carbonate; Yield given. Multistep reaction; 1.) MeCN, 50-55 deg C;

DOI:10.1016/S0040-4020(01)86056-7

upstream raw materials:

1H-imidazole