41546-31-0

Basic information

• Product Name: L-Xylofuranose (9CI)
• Synonyms: L-Xylofuranose (9CI)
• CAS NO: 41546-31-0
• Molecular Formula: C₅H₁₀O₅
• Molecular Weight: 150.1299
• Product Categories: CARBOHYDRATE
• Mol File: 41546-31-0.mol
• Article Data: 79

Chemical Properties

• Boiling Point: 375.4±42.0 °C(Predicted)
• Appearance: /
• Density: 1.681±0.06 g/cm3(Predicted)
• PKA: 12.16±0.70(Predicted)
• CAS DataBase Reference: L-Xylofuranose (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: L-Xylofuranose (9CI)(41546-31-0)
• EPA Substance Registry System: L-Xylofuranose (9CI)(41546-31-0)

Safety Data

• Hazardous Substances Data: 41546-31-0(Hazardous Substances Data)

Upstream product

• 42927-46-8 tetra-O-acetyl-D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 20881-04-3 1,2:3,5-di-O-isopropylidene-D-xylofuranose 
• 2280-44-6 D-Glucose 
• 61826-42-4 tetra-O-acetyl-D-arabinofuranose 
• 25152-95-8 3'-O-acetyl-N-benzoyl-2'-deoxyadenosine 
• 99677-75-5 4,5'-anhydro-3-(2,3-O-isopropylidene-β-D-ribofuranosyl)-4-hydroxyhexahydropyrimidine-2-thione 
• 6711-37-1 N⁶,N⁶-dibenzoyldeoxyadenosine 
• 104769-16-6 N⁶-benzoyl-5'-O-benzoyl-2'-deoxyadenosine 
• 958-09-8 2'-deoxy-D-adenosine 
• 58-61-7 adenosine 
• 93-87-8 D-ribose 5-phosphate 
• 58-63-9 Inosine 
• 32252-05-4 p-nitrophenylriboside 

Downstream Products

• 53829-60-0 1,2-O-isopropylidene-α-D-xylofuranose-3,5-phenylboronate 
• 4945-58-8 piperidino N-β-D-riboside 
• 5328-63-2 methyl-β-D-arabinopyranoside 
• 91-09-8 (2S,3S,4R,5R)-2-Methoxy-tetrahydro-pyran-3,4,5-triol 
• 25129-51-5 methyl β-D-arabinofuranoside 
• 56607-40-0 methyl D-arabinofuranoside 
• 1824-96-0 methyl ribofuranoside 
• 7473-45-2 1-O-methyl-D-ribofuranose 
• 52485-92-4 methyl α-D-ribofuranoside 
• 98-01-1 furfural 
• 64-18-6 formic acid 
• 79-14-1 glycolic Acid 
• 849585-22-4 LACTIC ACID 
• 64-19-7 acetic acid 

Relevant articles and documents

New triterpenoid saponin from the stems of Albizia adianthifolia (Schumach.) W.Wight

As part of our continuing study of apoptosis-inducing saponins from Cameroonian Albizia genus, one new triterpenoid saponin, named adianthifolioside J (1), together with the known gummiferaoside E (2), were isolated from Albizia adianthifolia stems. The s

Oleanane-type saponins and prosapogenins from Albizia julibrissin and their cytotoxic activities

Two undescribed oleanane-type saponins, julibrosides K–L, along with three undescribed oleanane-type prosapogenins, julibrosides M–O, were isolated from the stem bark of Albizia julibrissin Durazz. and the mild alkaline hydrolysate of the total saponin, r

New dammarane-type triterpenoid saponins from Panax notoginseng leaves and their nitric oxide inhibitory activities

Inflammation is a very common and important pathological process that can cause many diseases. The discovery of anti-inflammatory drugs and the treatment of inflammation are particularly essential. Dammarane-type triterpenoid saponins (PNS) were demonstrated to show anti-inflammatory effects in the leaves of Panax notoginseng. Chromatographies and spectral analysis methods were combined to isolate and identify PNS. Moreover, the nitric oxide (NO) inhibitory activities of all compounds were examined in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. As a result, eleven new dammarane-type triterpenoid saponins, notoginsenosides NL-A1-NL-A4 (1-4), NL-B1-NL-B3 (5-7), NL-C1-NL-C3 (8-10), and NL-D (11) were isolated, and their structures were identified by using various spectrometric techniques and chemical reactions. Among them, compounds 4 and 11 were characterized by the malonyl substitution at 3-position. The 3-malonyl substituted dammarane-type terpennoids were first obtained from natural products. In addition, compounds 1, 2, 5, 6, and 8-10 were found to play an important role in suppressing NO levels at 50 μM, without cytotoxicity. All inhibitory activities were found to be dose-dependent.