(2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid

Base Information

• Chemical Name: (2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid
• CAS No.: 24587-32-4
• Molecular Formula: C₇H₁₂N₂O₄
• Molecular Weight: 188.183
• Hs Code.: 2933990090
• UNII: 1YZZ05TOK3
• Nikkaji Number: J908.021J
• Mol file: 24587-32-4.mol

Synonyms:Gly-4-hydroxy-Pro;Gly-Hyp;glycyl-4-hydroxyproline

Chemical Property of (2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid

Chemical Property:

• Vapor Pressure: 1.81E-11mmHg at 25°C
• Refractive Index: 1.6
• Boiling Point: 485.6 °C at 760 mmHg
• PKA: 2.97±0.40(Predicted)
• Flash Point: 247.5 °C
• PSA: 103.86000
• Density: 1.518 g/cm³
• LogP: -1.37030
• Storage Temp.: -15°C
• Solubility.: Aqueous Acid (Slightly), Water (Slightly, Sonicated)
• XLogP3: -4.3
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 188.07970687
• Heavy Atom Count: 13
• Complexity: 231

Purity/Quality:

97% ^*data from raw suppliers

(2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(CN(C1C(=O)O)C(=O)CN)O
• Isomeric SMILES: C1[C@H](CN([C@@H]1C(=O)O)C(=O)CN)O
• Uses: (2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic Acid is a reagent in the study of acrylproline cleavage by prolidase enzymes.

Technology Process of (2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic acid

There total 6 articles about (2S,4R)-1-(2-Aminoacetyl)-4-hydroxypyrrolidine-2-carboxylic 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:

1-chloroacetyl-4-oxy-L-proline → trans-1-glycyl-4-hydroxy-L-proline (24587-32-4)

Guidance literature:

With ammonia; at 37 ℃;

Reference yield:

N-(N-benzyloxycarbonylglycyl)-4-hydroxy-L-proline (22029-01-2) → trans-1-glycyl-4-hydroxy-L-proline (24587-32-4)

Guidance literature:

With methanol; palladium; acetic acid; Hydrogenation;

Reference yield:

cis-1-(N-benzyloxycarbonyl-glycyl)-4-hydroxy-L-proline (22029-01-2) → cis-1-glycyl-4-hydroxy-L-proline (24587-32-4)

Guidance literature:

With methanol; palladium; acetic acid; Hydrogenation;

upstream raw materials:

N-(N-benzyloxycarbonylglycyl)-4-hydroxy-L-proline

4R-4-hydroxyproline

cis-1-(N-benzyloxycarbonyl-glycyl)-4-hydroxy-L-proline

hydroxy L-proline

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