Alanine, N-(1-carboxyethyl)-, (R*,R*)-

Base Information

• Chemical Name: Alanine, N-(1-carboxyethyl)-, (R*,R*)-
• CAS No.: 101541-15-5
• Molecular Formula: C₆H₁₁NO₄
• Molecular Weight: 161.158
• UNII: 20QBE05XDW
• Wikidata: Q27117012
• Metabolomics Workbench ID: 55523
• Mol file: 101541-15-5.mol

Synonyms:101541-15-5;Alanine, N-(1-carboxyethyl)-, (R*,R*)-;N-(1-Carboxyethyl)alanine, DL-;20QBE05XDW;103954-11-6;D-Alanine, N-(1-carboxyethyl)-, (R)- (9CI);(R,R)-2,2'-iminodipropanoic acid;(2R)-2-[[(1R)-1-carboxyethyl]amino]propanoic acid;Alanine, N-(1-carboxyethyl)-, (R*,R*)- (9CI);(2R,2'R)-2,2'-iminodipropanoic acid;(2R,2'R)-2,2'-azanediyldipropanoic acid;DL-Alanine, N-(1-carboxyethyl)-, (R*,R*)-;UNII-20QBE05XDW;DL-N-(1-carboxyethyl)alanine;SCHEMBL4572680;CHEBI:37027;Q27117012

Chemical Property of Alanine, N-(1-carboxyethyl)-, (R*,R*)-

Chemical Property:

• PSA: 86.63000
• LogP: -0.08690
• XLogP3: -2.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 161.06880783
• Heavy Atom Count: 11
• Complexity: 150

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

Technology Process of Alanine, N-(1-carboxyethyl)-, (R*,R*)-

There total 1 articles about Alanine, N-(1-carboxyethyl)-, (R*,R*)- 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:

→ racem.-2,2'-imino-dipropionic acid (19149-54-3,65621-33-2,73890-66-1,92283-80-2,101541-15-5,103954-11-6)

Guidance literature:

Gewinnung aus den optischen Antipoden;

DOI:10.1002/hlca.19420250318