800379-24-2

Basic information

• Product Name: alpha-D-Xylofuranuronicacid,3-amino-3-deoxy-1,2-O-(1-methylethylidene)-,methylester(9CI)
• Synonyms: alpha-D-Xylofuranuronicacid,3-amino-3-deoxy-1,2-O-(1-methylethylidene)-,methylester(9CI)
• CAS NO: 800379-24-2
• Molecular Formula: C₉H₁₅NO₅
• Molecular Weight: 217.2191
• Product Categories: METHYL
• Mol File: 800379-24-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 275.1±40.0 °C(Predicted)
• Appearance: /
• Density: 1.208±0.06 g/cm3(Predicted)
• PKA: 6.43±0.60(Predicted)
• CAS DataBase Reference: alpha-D-Xylofuranuronicacid,3-amino-3-deoxy-1,2-O-(1-methylethylidene)-,methylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-D-Xylofuranuronicacid,3-amino-3-deoxy-1,2-O-(1-methylethylidene)-,methylester(9CI)(800379-24-2)
• EPA Substance Registry System: alpha-D-Xylofuranuronicacid,3-amino-3-deoxy-1,2-O-(1-methylethylidene)-,methylester(9CI)(800379-24-2)

Safety Data

• Hazardous Substances Data: 800379-24-2(Hazardous Substances Data)

Upstream product

• 1060716-74-6 methyl 3-azido-3-deoxy-1,2-O-(1-methylethylidne)-α-D-xylofuranoate 
• 13964-23-3 3-azido-3-deoxy-1,2:5,6-di-(O-isopropylidene)-α-D-glucofuranose 
• 22169-71-7 (R)-1-((3aR,5S,6S,6aR)-6-azido-2,2-dimethyltetrahydrofuro-[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol 
• 800379-17-3 (3aR,5S,6R,6aR)-6-azido-2,2-dimethyltetrahydrofuro[2,3-d][1,3]-dioxole-5-carboxylic acid 
• 1204773-09-0 C₁₄H₂₃NO₇ 

Downstream Products

• 1060716-76-8 methyl 3-{[N²-(tert-butoxycarbonyl)-N⁵-(phenoxycarbonyl)-L-ornithyl]amino}-3-deoxy-1,2-O-(1-methylethylidene)-α-D-xylofuranoate 

Relevant articles and documents

Formation of a stable 14-helix in short oligomers of furanoid cis-β-sugar-amino acid

Oligomers of a new class of sugar amino acids (SAA) using a xylofuranoic acid has been shown to generate a robust 14-helix. The design involved the use of xylofuranose with a cis arrangement between the amine and carboxyl groups to promote the adoption of a 14-helix instead of a mixed 12/10-helix observed in a sugar oligomer using a ribofuranoic acid and β-Ala. The observation of a stable right-handed 14-helix in a cis-SAA is unprecedented. Copyright

Synthesis and conformational studies of a hybrid cyclic peptide based on cis-β-furanoid sugar amino acid (FSAA) and ornithine

The conformational control of a 14-helix nucleating template, cis-β-furanoid sugar amino acid (FSAA), over a flexible δ-amino acid, ornithine is studied in a FSAA-ornithine cyclic tetrapeptide. Extensive NMR and MD studies reveal that the cyclic peptide adopts a three-dimentional bowl-shape cavity, which promotes six- and seven-membered intra- and inter-residue H-bonding, in polar and nonpolar solvents, respectively.