6696-41-9

Basic information

• Product Name: 6-DEOXY-L-GALACTOPYRANOSE
• Synonyms: 6-DEOXY-L-GALACTOPYRANOSE;6-DEOXY-L-GALACTOSE;6-DEOXY-ALPHA-L-GALACTOSE;3,4,5-TRIS-BENZYLOXY-2-METHYL-6-P-TOLYLSULFANYL-TETRAHYDRO-PYRAN;L-FUC;L-(-)-FUCOSE;L-FUCOSE;L-(-)-Fucose,97%
• CAS NO: 6696-41-9
• Molecular Formula: C₆H₁₂O₅
• Molecular Weight: 164.16
• EINECS: 219-452-7
• Mol File: 6696-41-9.mol
• Article Data: 34

Chemical Properties

• Melting Point: 136-140°C
• Boiling Point: 323.9°C at 760 mmHg
• Flash Point: 149.7°C
• Appearance: /
• Density: 1.556g/cm³
• Vapor Pressure: 1.99E-05mmHg at 25°C
• Refractive Index: 1.593
• Storage Temp.: Store at RT.
• Sensitive: Hygroscopic
• Merck: 14,4279
• BRN: 1422661
• CAS DataBase Reference: 6-DEOXY-L-GALACTOPYRANOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-DEOXY-L-GALACTOPYRANOSE(6696-41-9)
• EPA Substance Registry System: 6-DEOXY-L-GALACTOPYRANOSE(6696-41-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-27-36/37/39
• Hazardous Substances Data: 6696-41-9(Hazardous Substances Data)

Usage

Definition

ChEBI: An L-fucopyranose having alpha-configuration at the anomeric centre.

InChI:InChI=1/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6-/m0/s1

Upstream product

• 67-56-1 methanol 
• 1099684-82-8 p-cyanophenyl α-L-fucopyranoside 
• 10231-84-2 (4-nitro-phenyl)-α-L-fucopyranoside 
• 157843-41-9 2-chloro-4-nitrophenyl α-L-fucopyranoside 
• 18156-74-6 1-(Trimethylsilyl)imidazole 
• 55804-74-5 clitorin 
• 55696-57-6 manghaslin 
• 1668-08-2 L-galactono-1,4-lactone 
• 24286-28-0 (3S,4S,5R)-dihydro-3,4-dihydroxy-5-((1'S)-1'-hydroxyethyl)furan-2(3H)-one 
• 1372946-80-9 methyl 6-bromo-6-deoxy-L-galactonate 
• 210100-16-6 6-bromo-6-deoxy-L-galactonolactone 
• 1226-39-7 p-nitrophenyl-β-D-fucopyranoside 
• 88434-20-2 6α-O-[β-D-galactopyranosyl-(1→3)-β-D-fucopyranosyl-(1→2)-β-D-galactopyranosyl-(1→4)-[β-D-quinovopyranosyl-(1→2)]-β-D-xylopyranosyl-(1→3)-β-D-quinovopyranosyl]-20-hydroxy-23-one-5α-cholest-9(11)-en-3β-yl sodium sulfate 
• 107091-09-8 3-O-β-D-galactopyranosyl-(1->2)-<β-D-xylopyranosyl-(1->3)>-β-D-glucuronopyranosyl quillaic acid 28-O-β-D-apiofuranosyl-(1->3)-β-D-xylopyranosyl-(1->4)-<β-D-glucopyranosyl-(1->3)>-α-L-rhamnopyranosyl-(1->2)-β-D-fucopyranoside. 

Downstream Products

• 53829-55-3 α-L-Furopyranose 1,2 : 3,4-bis(butanboronat) 
• 53829-56-4 O¹,O²;O³,O⁴-bis-phenylboranediyl-α-L-6-deoxy-galactopyranose 
• 65310-00-1 (3S,4R,5S,6S)-2-methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol 
• 57472-03-4 methyl β-L-fucofuranoside 
• 57472-02-3 methyl α-L-fucofuranoside 
• 14687-15-1 methyl L-fucopyranoside 
• 1128-40-1 methyl β-L-fucopyranoside 
• 1128-40-1 methyl 6-deoxy-β-D-galactopyranoside 
• 1128-40-1 methyl α-D-fucopyranoside 
• 14917-55-6 methyl 6-deoxy-α-L-mannopyranoside 
• 139523-48-1 (2S,3S,4S,5S)-1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-hexane-2,3,4,5-tetraol 
• 80483-13-2 2,3,4-tri-O-acetyl-L-fucopyranosyl bromide 
• 5328-43-8 1-deoxy-L-galactitol 
• 95120-27-7 6-Deoxy-β-D-allofuranosid 

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

Melanogenesis-Inhibitory and Cytotoxic Activities of Triterpene Glycoside Constituents from the Bark of Albizia procera

Five oleanane-type triterpene glycosides including three new ones, proceraosides E-G (1-3), were isolated from a MeOH-soluble extract of Albizia procera bark. The structures of 1-3 were determined by use of NMR spectra, HRESIMS, and chemical methods. Compounds 1-5 exhibited inhibitory activities against the proliferation of the A549, SKBR3, AZ521, and HL60 human cancer cell lines (IC50 0.28-1.8 μM). Additionally, the apoptosis-inducing activity of compound 2 was evaluated by Hoechst 33342 staining and flow cytometry, while the effects of 2 on the activation of caspases-9, -8, and -3 in HL60 cells were revealed by Western blot analysis.