14795-83-6

Basic information

• Product Name: alpha-D-Xylofuranose(9CI)
• Synonyms: alpha-D-Xylofuranose(9CI)
• CAS NO: 14795-83-6
• Molecular Formula: C₅H₁₀O₅
• Molecular Weight: 150.13
• Product Categories: CARBOHYDRATE
• Mol File: 14795-83-6.mol
• Article Data: 78

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: alpha-D-Xylofuranose(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-D-Xylofuranose(9CI)(14795-83-6)
• EPA Substance Registry System: alpha-D-Xylofuranose(9CI)(14795-83-6)

Safety Data

• Hazardous Substances Data: 14795-83-6(Hazardous Substances Data)

Upstream product

• 524-69-6 adenine xyloside 
• 42927-46-8 tetra-O-acetyl-D-xylofuranose 
• 20881-04-3 1,2:3,5-di-O-isopropylidene-D-xylofuranose 
• 1824-96-0 methyl α-D-xylofuranoside 
• 2280-44-6 D-Glucose 
• 3228-71-5 9-(α-D-arabinofuranosyl)adenine 
• 61826-42-4 tetra-O-acetyl-D-arabinofuranose 
• 68768-32-1 3-methylguanosine 
• 30802-00-7 hydroxycinnamoyl-S-CoA 
• 50-00-0 formaldehyd 
• 25152-95-8 3'-O-acetyl-N-benzoyl-2'-deoxyadenosine 
• 50908-04-8 (-)-Methyl-5-O-trityl-β-D-ribofuranosid 
• 2627-69-2 AICA riboside 
• 87424-20-2 2'-deoxy-N⁶-[(9H-fluoren-9-ylmethoxy)carbonyl]adenosine 

Downstream Products

• 52572-01-7 α-D-Xylofuranose 1,2 : 3,5-bis(butanboronat) 
• 27963-98-0 2-amino-β-D-arabinofurano[1',2':4,5]-oxazoline 
• 53829-60-0 1,2-O-isopropylidene-α-D-xylofuranose-3,5-phenylboronate 
• 4945-58-8 piperidino N-β-D-riboside 
• 100604-20-4 (3aS,5R,6S,6aR)-2-<2,3,3a,5,6,6a-Hexahydro-6-hydroxy-5-(hydroxymethyl)furo<2,3-d>oxazol-2-yliden>cyanessigsaeure-methylester 
• 1824-97-1 methyl β-D-xylofuranoside 
• 1824-96-0 methyl xylofuranoside 
• 98-01-1 furfural 
• 64-18-6 formic acid 
• 79-14-1 glycolic Acid 
• 849585-22-4 LACTIC ACID 
• 64-19-7 acetic acid 
• 127-17-3 2-oxo-propionic acid 
• 51754-99-5 Methyl 3,5-O-Isopropylidene-β-D-xylofuranoside 

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

Lebbeckoside C, a new triterpenoid saponin from the stem barks of Albizia lebbeck inhibits the growth of human glioblastoma cells

One new acacic acid-type saponin, named lebbeckoside C (1), was isolated from the stem barks of Albizia lebbeck. Its structure was established on the basis of extensive analysis of 1D and 2D NMR (1H, 13C NMR, DEPT, COSY, TOCSY, ROESY, HSQC and HMBC) experiments, HRESIMS studies, and by chemical evidence as 3-O-[β-d-xylopyranosyl-(l→2)-β-d-fucopyranosyl-(1→6)-[β-d-glucopyranosyl(1→2)]-β-d-glucopyranosyl]-21-O-{(2E,6S)-6-O-{4-O-[(2E,6S)-2,6-dimethyl-6-O-(β-d-quinovopyranosyl)octa-2,7-dienoyl]-4-O-[(2E,6S)-2,6-dimethyl-6-O-(β-d-quinovopyranosyl)octa-2,7-dienoyl]-β-d-quinovopyranosyl}-2,6-dimethylocta-2,7-dienoyl}acacic acid 28 O-[β-d-quinovopyranosyl-(l→3)-[α-l-arabinofuranosyl-(l→4)]-α-l-rhamnopyranosyl-(l→2)-β-d-glucopyranosyl] ester. The isolated saponin (1) displayed significant cytotoxic activity against the human glioblastoma cell line U-87 MG and TG1 stem-like glioma cells isolated from a patient tumor with IC50 values of 1.69 and 1.44?μM, respectively.