Ribose-5-phosphate

Base Information

• Chemical Name: Ribose-5-phosphate
• CAS No.: 3615-55-2
• Molecular Formula: C₅H₁₁O₈P
• Molecular Weight: 230.111
• European Community (EC) Number: 224-310-2
• UNII: 4B2428FLTO
• DSSTox Substance ID: DTXSID10897600
• Nikkaji Number: J205.693C
• Wikipedia: Ribose_5-phosphate
• Wikidata: Q418855
• Metabolomics Workbench ID: 49968
• Mol file: 3615-55-2.mol

Synonyms:D-ribose 5-phosphate;D-ribose-5-phosphoric acid;ribose 5-monophosphate;ribose 5-phosphate;ribose phosphate;ribose-5-phosphate;ribose-5-phosphoric acid;ribose-5-phosphoric acid, (D-ribofuranose)-isomer;ribose-5-phosphoric acid, (D-ribose)-isomer;ribose-5-phosphoric acid, monobarium salt, (D-ribose)-isomer;ribose-5-phosphoric acid, monosodium salt, (D-ribose)-isomer

Chemical Property of Ribose-5-phosphate

Chemical Property:

• Boiling Point: 559.1°Cat760mmHg
• Flash Point: 291.9°C
• PSA: 154.33000
• Density: 1.803g/cm³
• LogP: -2.62270
• XLogP3: -3.4
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 6
• Exact Mass: 230.01915430
• Heavy Atom Count: 14
• Complexity: 224

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(C(C(C=O)O)O)O)OP(=O)(O)O
• Isomeric SMILES: C([C@H]([C@H]([C@H](C=O)O)O)O)OP(=O)(O)O

Technology Process of Ribose-5-phosphate

There total 24 articles about Ribose-5-phosphate 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:

→ D-ribose 5-phosphate (3615-55-2,7591-07-3,13137-52-5,66768-39-6,69881-36-3,69881-39-6,136376-80-2,136376-83-5,136376-85-7,136376-88-0,136376-89-1,4300-28-1)

Guidance literature:

With water; in Gegenwart eines sauren Kationenaustaschers;

DOI:10.1021/ja01650a075

Reference yield:

→ D-ribose 5-phosphate (3615-55-2,7591-07-3,13137-52-5,66768-39-6,69881-36-3,69881-39-6,136376-80-2,136376-83-5,136376-85-7,136376-88-0,136376-89-1,4300-28-1)

Guidance literature:

With hydrogenchloride;

Reference yield:

D-ribose (50-69-1) → D-ribose 5-phosphate (3615-55-2,7591-07-3,13137-52-5,66768-39-6,69881-36-3,69881-39-6,136376-80-2,136376-83-5,136376-85-7,136376-88-0,136376-89-1,4300-28-1)

Guidance literature:

With hydrogenchloride; Ammonium 9,10-Dihydro-9,10-phenanthrenediol Cyclic Phosphate; In N,N-dimethyl-formamide;

upstream raw materials:

[5']inosinic acid

D-ribose

D-ribose 5-phosphate

D-ribose 5-phosphate

Downstream raw materials:

5-phosphoribosylamine

O⁵-Trihydroxydiphosphoryl-D-ribose

O⁵-Tetrahydroxytriphosphoryl-D-ribose

D-ribitol-5-phosphate

Refernces

• 1、 Drueckhammer, Dale G.,Durrwachter, J. Robert,Pederson, Richard L.,Crans, Debbie C.,Daniels, Lacy,Wong, Chi-Huey. "Reversible and in Situ Formation of Organic Arsenates and Vanadates as Organic Phosphate Mimics in Enzymatic Reactions: Mechanistic Investigation of Aldol Reactions and Synthetic Applications". . p. 70 - 77. Retrieved 2007/10/02.
• 2、 Pierce, John,Serianni, Anthony S.,Barker, Robert. "Anomerization of Furanose Sugars and Sugar Phosphates". . p. 2448 - 2456. Retrieved 2007/10/02.