87372-47-2

Basic information

• Product Name: alpha-d-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), tetrasodium salt
• Synonyms: alpha-d-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), tetrasodium salt;Einecs 289-314-9
• CAS NO: 87372-47-2
• Molecular Formula: C₅H₉O₁₃P₃*4Na
• Molecular Weight: 868.066526
• EINECS: 289-314-9
• Mol File: 87372-47-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: alpha-d-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), tetrasodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-d-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), tetrasodium salt(87372-47-2)
• EPA Substance Registry System: alpha-d-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), tetrasodium salt(87372-47-2)

Safety Data

• Hazardous Substances Data: 87372-47-2(Hazardous Substances Data)

Upstream product

• 4578-31-8 adenosine-5'-monophosphate disodium salt 
• 108321-99-9 α,β-D-ribofuranose-5-phophate disodium salt 
• 532-20-7 D-Ribose 

Downstream Products

• 113599-16-9 5-phospho-α-D-ribofuranosyl 1,2-cyclic monophosphate 
• 113599-17-0 α-D-ribofuranosyl 1,5-biphosphate tetrasodium salt 
• 113599-19-2 α-D-ribofuranosyl 2,5-biphosphate tetrakis(cyclohexylammonium) salt 
• 3387-36-8 disodium uridine-5'-monophosphate 

Relevant articles and documents

Practical Synthesis of 5-Phospho-D-ribosyl α-1-pyrophosphate (PRPP): Enzymatic Routes from Ribose 5-Phosphate or Ribose

This paper describes enzymatic syntheses of 5-phospho-D-ribosyl α-1-pyrophosphate (PRPP) on a 75-mmol scale.The reactions used PAN-immobilized PRPP synthetase as catalyst with in situ ATP-cofactor regeneration.In one procedure pure r-5-P was used as a starting material; in a second, r-5-P was synthesized by ribokinase-catalyzed phosphorilation of D-ribose and used in situ.The potential for use of PRPP as a starting material for the preparation of nucleotides was demonstrated by an enzymatic synthesis of UMP.This paper also describes several methods for the preparation of r-5-P: acid-catalyzed hydrolysis of AMP, acid-catalyzed hydrolysis of crude mononucleotide mixture obtained by digestion of RNA, chemical synthesis from D-ribose, and ribokinase-catalyzed synthesis from D-ribose.Procedures are described for the isolation of PRPP synthetase (from Salmonella typhimurium) and ribokinase (from Lactobacillus plantarum) and for immobilization of these enzymes in PAN.