52630-68-9

Basic information

• Product Name: N-[(2R,3R,4R,5R)-4,5,6-trihydroxy-1-oxo-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-hexan-2-yl]acetamide
• Synonyms: 3-O-fucopyranosyl-2-acetamido-2-deoxyglucopyranose;N-[(2R,3R,4R,5R)-4,5,6-trihydroxy-1-oxo-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-hexan-2-yl]acetamide;2-(AcetylaMino)-2-deoxy-3-O-(6-deoxy-α-L-galactopyranosyl)-D-glucopyranose
• CAS NO: 52630-68-9
• Molecular Formula: C14H25NO10
• Molecular Weight: 367.35
• Product Categories: Oligosaccharides
• Mol File: 52630-68-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: >155°C (dec.)
• Boiling Point: 792.9°Cat760mmHg
• Flash Point: 433.3°C
• Appearance: /
• Density: 1.49g/cm³
• Storage Temp.: -20°C Freezer
• Stability: Hygroscopic
• CAS DataBase Reference: N-[(2R,3R,4R,5R)-4,5,6-trihydroxy-1-oxo-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-hexan-2-yl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(2R,3R,4R,5R)-4,5,6-trihydroxy-1-oxo-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-hexan-2-yl]acetamide(52630-68-9)
• EPA Substance Registry System: N-[(2R,3R,4R,5R)-4,5,6-trihydroxy-1-oxo-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyl-oxan-2-yl]oxy-hexan-2-yl]acetamide(52630-68-9)

Safety Data

• Hazardous Substances Data: 52630-68-9(Hazardous Substances Data)

Usage

Chemical Properties

White to Off-White Solid

Upstream product

• 116514-50-2 ethyl 2,3,4-tri-O-benzyl-1-thio-β-L-fucopyranoside 
• 78246-81-8 benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 196941-73-8 benzyl 2-acetamido-4,6-O-benzylidene-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-2-deoxy-α-D-glucopyranoside 
• 50711-25-6 benzyl 2-acetamido-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-2-deoxy-α-D-glucopyranoside 

Relevant articles and documents

Synthesis of mono- and di-α-l-fucosylated 2-acetamido-2-deoxy-N-glycyl-β-d-glucopyranosylamines, spacered fragments of glycans of N-glycoproteins

α-l-Fucp-(1→3)-d-GlcNAc, α-l-Fucp-(1→6)-[α-l-Fucp-(1→3)]-d-GlcNAc, and β-d-Galp-(1→3)-[α-l-Fucp-(1→4)]-d-GlcNAc were converted into corresponding β-glycopyranosylamines by action of ammonium carbamate in aqueous boric acid, or in aqueous methanol in case