20881-87-2

Basic information

• Product Name: Methyl 4-amino-4,6-dideoxy-α-D-mannopyranoside
• Synonyms: Methyl 4-amino-4,6-dideoxy-α-D-mannopyranoside
• CAS NO: 20881-87-2
• Molecular Formula: C7H15NO4
• Molecular Weight: 177.1983
• Mol File: 20881-87-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 313.2°C at 760 mmHg
• Flash Point: 143.2°C
• Appearance: /
• Density: 1.26g/cm³
• Vapor Pressure: 4.39E-05mmHg at 25°C
• Refractive Index: 1.516
• CAS DataBase Reference: Methyl 4-amino-4,6-dideoxy-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-amino-4,6-dideoxy-α-D-mannopyranoside(20881-87-2)
• EPA Substance Registry System: Methyl 4-amino-4,6-dideoxy-α-D-mannopyranoside(20881-87-2)

Safety Data

• Hazardous Substances Data: 20881-87-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H15NO4/c1-3-4(8)5(9)6(10)7(11-2)12-3/h3-7,9-10H,8H2,1-2H3/t3-,4-,5+,6+,7+/m1/s1

Upstream product

• 20881-80-5 (2S,3S,4S,5S,6R)-5-azidotetrahydro-2-methoxy-6-methyl-2H-pyran-3,4-diol 
• 20197-44-8 Methyl 4-acetamido-2,3-di-O-acetyl-4,6-dideoxy-α-D-mannopyranoside 
• 117514-14-4 methyl 6-deoxy-4-O-(methylsulfonyl)-α-D-talopyranoside 
• 63167-69-1 methyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 104846-19-7 methyl 6-deoxy-2,3-O-isopropylidene-α-D-talopyranoside 
• 15830-63-4 methyl 6-deoxy-2,3-O-isopropylidene-α-D-lyxo-hexopyranosid-4-ulose 
• 15830-64-5 methyl 6-deoxy-2,3-O-isopropylidene-4-O-(methylsulfonyl)-α-D-talopyranoside 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 92735-13-2 methyl 4-azido-4-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 15856-44-7 Methyl 4-acetamido-4,6-dideoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 141232-01-1 Methyl 4-azido-4-deoxy-2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 135216-54-5 methyl 6-deoxy-4-O-(p-tolylsulfonyl)-α-D-mannopyranoside 
• 10515-99-8 methyl 6-deoxy-2,3-O-isopropylidene-4-O-(p-tolylsulfonyl)-α-D-mannopyranoside 

Downstream Products

• 116786-66-4 Methyl 4,6-Dideoxy-4-<(S)-2,4-dihydroxybutanamido>-α-D-mannopyranoside 
• 101072-27-9 Methyl 2,3-di-O-acetyl-4,6-dideoxy-4-<(1S)-(1,4/5,6)-4,5,6-triacetoxy-3-(benzoyloxymethyl)-2-cyclohexen-1-ylamino>-α-D-mannopyranoside 
• 92567-48-1 Methyl 2,3-di-O-acetyl-4,6-dideoxy-4-<(1S)-(1,4/2,3,5)-2,3,4-triacetoxy-5-(acetoxymethyl)-1-cyclohexylamino>-α-D-mannopyranoside 
• 15856-45-8 methyl 4-acetamido-4,6-dideoxy-α-D-mannopyranoside 
• 116786-66-4 methyl 4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-mannopyranoside 
• 141316-50-9 Methyl 4,6-dideoxy-4-<(1S)-(1,4/5,6)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-ylamino>-α-D-mannopyranoside 

Relevant articles and documents

Synthesis of the Methyl α-D-Glycosides of Amicetose, Perosamine and Janose

New methods for the synthesis of tri- and di-deoxy sugar, namely methyl α-D-amicetoside, methyl α-D-perosaminoside and methyl α-D-janoside are described.The readily available methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside has been used as chiral

The structures of pramidicins A, B, and C: A novel family of antifungal antibiotics

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SYNTHESIS OF ANTIGENIC DETERMINANTS OF THE Brucella A ANTIGEN, UTILIZING METHYL 4-AZIDO-4,6-DIDEOXY-α-D-MANNOPYRANOSIDE EFFICIENTLY DERIVED FROM D-MANNOSE

A strategy for the synthesis of Brucella O-antigenic determinants containing 2-linked 4,6-dideoxy-4-formamido-α-D-mannopyranosyl residues is described.The approach adopted also permits the N-acyl moiety to be varied.A high-yield synthesis of methyl 4-azid