N-Succinyl-5-aMinoiMidazole-4-carboxaMide Ribose

Base Information

• Chemical Name: N-Succinyl-5-aMinoiMidazole-4-carboxaMide Ribose
• CAS No.: 17388-80-6
• Molecular Formula: C₁₃H₁₈N₄O₉
• Molecular Weight: 374.307
• Mol file: 17388-80-6.mol

Synonyms:

Chemical Property of N-Succinyl-5-aMinoiMidazole-4-carboxaMide Ribose

Chemical Property:

• Melting Point: >205°C (dec.)
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: Water (Very Slightly, Heated)

Purity/Quality:

97% ^*data from raw suppliers

N-Succinyl-5-aminoimidazole-4-carboxamide Ribose ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Uses: A metabolite of Purine. Purine metabolism by adenylosuccinasedeficient. Since adenosine is a potent inhibitor of neuronal function, depressing the release of several excitatory transmitters and causin g direct hyperpolarization of neurons, it was possible that the symptoms seen in adenylosuccinate lyase (ASase) deficient patients could reflect an interference of succinylpurines with neurotransmissi on. N-Succinyl-5-aminoimidazole-4-carboxamide Ribose is used in the detection of adenylosuccinate lyase deficiency in infants and mice as it is seen as a significant indicator in autism diagnosis.

Technology Process of N-Succinyl-5-aMinoiMidazole-4-carboxaMide Ribose

There total 1 articles about N-Succinyl-5-aMinoiMidazole-4-carboxaMide Ribose 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:

→ 5-Amino-1-β-D-ribofuranosyl-imidazol-carbonsaeure-(4)-(1,2-dicarboxy-ethylamid) (17388-80-6,96192-28-8)

Guidance literature:

5-Amino-1-(2,3-O-isopropyliden-β-D-ribofuranosyl)-imidazol-carbonsaeure-(4)-methylester, 1.) NaOH, 2.) Pentachlorphenol, Dicyclohexyl-carbodiimid, 3.) Chlorphosphorsaeure-dibenzylester, 4.) Diethyl-L-aspartat, 5.) CH3COOH;

DOI:10.1039/j39670001088

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