18784-01-5

Basic information

• Product Name: N¹-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide
• Synonyms: N¹-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide
• CAS NO: 18784-01-5
• Molecular Weight: 647.479
• Mol File: 18784-01-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N¹-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: N¹-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide(18784-01-5)
• EPA Substance Registry System: N¹-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide(18784-01-5)

Safety Data

• Hazardous Substances Data: 18784-01-5(Hazardous Substances Data)

Upstream product

• 98-92-0 nicotinamide 
• 22860-91-9 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 29706-90-9 β-D-2,3,5-tri-O-benzoylribofuranosyl chloride 

Downstream Products

• 1094-61-7 nicotinamide mononucleotide 
• 53-84-9 NAD 

Relevant articles and documents

Chemical synthesis method of NMN

The invention discloses a chemical synthesis method of NMN. The synthesis method comprises the following steps: firstly, enabling ribofuranose and niacinamide to react; then enabling a generated compound to react with metaphosphate; after reacting, acidifying; and then purifying to obtain the high-purity NMN. Compared with enzymatic reaction, the synthesis method disclosed by the invention has the advantages of low raw material cost, moderate and stable technological conditions and easiness for controlling; indexes of products of different batches are close and the reaction productivity is easy to improve; and compared with a fermentation method, the product obtained by the preparation method has high safety and the application prospect of the product is improved.