113421-71-9

Basic information

• Product Name: 5-deoxy-β-L-ribose
• CAS NO: 113421-71-9
• Molecular Weight: 134.132
• Mol File: 113421-71-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 5-deoxy-β-L-ribose(CAS DataBase Reference)
• NIST Chemistry Reference: 5-deoxy-β-L-ribose(113421-71-9)
• EPA Substance Registry System: 5-deoxy-β-L-ribose(113421-71-9)

Safety Data

• Hazardous Substances Data: 113421-71-9(Hazardous Substances Data)

Upstream product

• 18555-65-2 L-5-deoxy-ribose 
• 76647-70-6 (3R,4R,5S)-3,4-dihydroxy-5-methyldihydrofuran-2(3H)-one 
• 93978-94-0 5-deoxy-L-ribose 
• 184430-10-2 2,2-Dimethyl-propionic acid (2S,3S,4R)-4-(2,2-dimethyl-propionyloxy)-2-methyl-5-oxo-tetrahydro-furan-3-yl ester 
• 184430-09-9 (2R,3R)-2,3-Bis-(2,2-dimethyl-propionyloxy)-4-oxo-butyric acid methyl ester 
• 141314-94-5 (2R,3R)-methyl 4-chloro-4-oxo-2,3-dipivaloxybutanoate 
• 4159-66-4 (R)-1-((4R,5S)-5-((S)-1-hydroxyethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethane-1,2-diol 
• 93978-94-0 5-deoxy-L-arabinose 
• 38279-72-0 2,3-cyclohexylidene-5-deoxy-L-ribose 
• 4152-76-5 1-(6-amino-purin-9-yl)-β-D-1,5-dideoxy-arabinofuranose 
• 13039-56-0 5-deoxy-L-arabinose 
• 27821-07-4 1,2,3-tri-O-acetyl-5-deoxy-β-D-ribofuranose 

Downstream Products

• 93978-94-0 5-deoxy-L-arabinose 
• 93978-94-0 5-deoxy-L-ribose 
• 62933-57-7 1',2'-O-diacetyl-L-biopterin 
• 22150-76-1 L-erythro biopterin 
• 22150-76-1 biopterin 
• 81827-31-8 2-N-acetyl-1',2'-di-O-acetyl-L-erythro-biopterin 
• 123168-30-9 5-deoxy-L-ribose phenylhydrazone 
• 18555-65-2 L-5-deoxy-ribose 
• 13039-56-0 5-deoxy-L-arabinose 

Relevant articles and documents

Effect of the Structure of the Glycon on the Acid-Catalyzed Hydrolysis of Adenine Nucleosides

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NOVEL PROCESS FOR THE PREPARATION OF SAPROPTERIN DIHYDROCHLORIDE AND ITS KEY INTERMEDIATE, L-BIOPTERIN

The present invention relates to a novel process for the preparation of Sapropterin dihydrochloride of formula (1) and its key intermediate L-erythro-biopterin of formula (2). The present process is a simple and economically viable process for commercial production of Sapropterin dihydrochloride of formula (1) and its key intermediate L-biopterin of formula (2).

Highly α-selective hydrolysis of α,β-epoxyalcohols using tetrabutylammonium fluoride

We report a simple method for the highly regio- and stereoselective hydrolysis of α,β-epoxyalcohols. Treatment of enantiopure epoxyalcohols derived from Sharpless epoxidation with TBAF/H2O resulted in exclusive ring opening at the normally disfavored α-position, providing access to arabino- or lyxo-configured triols with full preservation of stereochemical purity. The method was applied in syntheses of 5-deoxy-l-arabinose (26) and a family of bicyclic acetals based on the insect pheromone hydroxybrevicomin (4).