7388-99-0

Basic information

• Product Name: 1-Amino-1-deoxy-β-D-mannopyranose
• Synonyms: 1-Amino-1-deoxy-β-D-mannopyranose;β-D-Mannopyranosylamine;beta-D-MannopyranosylaMine
• CAS NO: 7388-99-0
• Molecular Formula: C₆H₁₃NO₅
• Molecular Weight: 179.17112
• Product Categories: 1-Amino-1-deoxy-β-D-mannopyranose is a small stereospecific carbohydrate.
• Mol File: 7388-99-0.mol

Chemical Properties

• Boiling Point: 416.4°Cat760mmHg
• Flash Point: 205.6°C
• Appearance: /
• Density: 1.563g/cm³
• Vapor Pressure: 1.12E-08mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: 1-Amino-1-deoxy-β-D-mannopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Amino-1-deoxy-β-D-mannopyranose(7388-99-0)
• EPA Substance Registry System: 1-Amino-1-deoxy-β-D-mannopyranose(7388-99-0)

Safety Data

• Hazardous Substances Data: 7388-99-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H13NO5/c7-6-5(11)4(10)3(9)2(1-8)12-6/h2-6,8-11H,1,7H2/t2-,3-,4+,5+,6-/m1/s1

Upstream product

• 530-26-7 D-Mannose 
• 65864-60-0 2,3,4,6-tetra-O-acetyl-1-azido-1-deoxy-β-D-mannopyranose 
• 65864-61-1 β-D-mannopyranosyl azide 

Downstream Products

• 74761-71-0 N-<(6-benzyloxycarbonylamino)hexanoyl>-β-D-mannopyranosylamine 
• 368886-89-9 (1,2-dideoxy-β-D-mannopyranoso)[1,2-d]oxazolidine-2-thione 
• 714968-87-3 N-(β-D-mannopyranosyl)-N'-phenylselenourea 
• 33758-19-9 N-bromoacetyl-β-D-mannopyranosylamine 
• 67283-56-1 N-ε-aminocaproyl-β-D-mannopyranosylamine 
• 134107-86-1 (1,2-dideoxy-β-D-mannopyranoso)[1,2-d]oxazolidin-2-one 
• 10163-09-4 (3,4,6-tri-O-acetyl-1,2-dideoxy-β-D-mannopyranoso)[1,2-d]oxazolidin-2-one 

Relevant articles and documents

The effect of monosaccharides on self-assembly of benzenetricarboxamides

The interaction between monosaccharides exhibits an important role in the assembly of monosaccharide-containing molecules. In this work, three common monosaccharides, glucose, galactose and mannose, are employed to investigate the effect of monosaccharide on the self-assembly of benzenetricarboxamide (BTA) core-containing molecules. In the presence of monosaccharides, three benzenetricarboxamide derivatives aggregate into different ordered structures. When alanine linkers are introduced to these molecules between the core and the monosacchride, morphologies of three types of monosaccharide BTAs turned to disordered, meanwhile their structures become similar with the increase of the length of alanine linkers, indicating the disappearance of the monosaccharide effects.

Fmoc-protected, glycosylated asparagines potentially useful as reagents in the solid-phase synthesis of N-glycopeptides

1-Amino 1-deoxy derivatives of unprotected O-β-D-galactopyranosyl-(1 → 3)-2-acetamido-2-deoxy-β-D-glucopyranose, 2-acetamido-2-deoxy-D-galactose, D-galactose, lactose, D-fucose, D-mannose, and 2-deoxy-D-arabino-hexose were prepared and acylated with N-flu