7284-37-9

Basic information

• Product Name: beta-D-Glucopyranosylamine
• Synonyms: BETA-D-GLUCOPYRANOSYLAMINE;1-AMINO-1-DEOXY-BETA-D-GLUCOSE;?D-Glucopyranosylamine;1-Amino-1-deoxy-?D-glucose;1-amino-1-deoxy-B-D-glucose;b-D-Glucopyranosylamine;glucopyranosylamine;(2R,3R,4S,5S,6R)-2-amino-6-(hydroxymethyl)oxane-3,4,5-triol
• CAS NO: 7284-37-9
• Molecular Formula: C₆H₁₃NO₅
• Molecular Weight: 179.17
• Mol File: 7284-37-9.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 416.4 °C at 760 mmHg
• Flash Point: 205.6 °C
• Appearance: /
• Density: 1.563 g/cm³
• Vapor Pressure: 1.12E-08mmHg at 25°C
• Refractive Index: 1.6
• Storage Temp.: 2-8°C
• Solubility: Aqueous Acid (Slightly), Methanol (Slightly), Water (Slightly)
• PKA: 13.19±0.70(Predicted)
• CAS DataBase Reference: beta-D-Glucopyranosylamine(CAS DataBase Reference)
• NIST Chemistry Reference: beta-D-Glucopyranosylamine(7284-37-9)
• EPA Substance Registry System: beta-D-Glucopyranosylamine(7284-37-9)

Safety Data

• Hazardous Substances Data: 7284-37-9(Hazardous Substances Data)

Usage

Uses

beta-D-Glucopyranosylamine

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

• 492-61-5 β-D-glucose 
• 41355-50-4 2,3,4,6-tetra-O-acetyl-D-glucosyl-1-amine 
• 20379-59-3 D-glucopyranosyl azide 
• 100639-11-0 N-(β-D-glucopyranosyl)triphenylphosphine imide 
• 2280-44-6 D-Glucose 
• 849367-23-3 (3aS,5R,6S,7S,7aR)-5-Hydroxymethyl-2-methyl-5,6,7,7a-tetrahydro-3aH-pyrano[2,3-d]oxazole-6,7-diol 
• 525589-11-1 2-methyl-4,5-dihydro-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyrano)[2,1-d]-2-oxazoline 
• 13992-25-1 1-azido-1-deoxy-β-D-glucopyranoside tetraacetate 
• 50-99-7 D-glucose 
• 604-69-3 β-D-glucose pentaacetate 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 6983-36-4 N-acetyl-β-D-glucopyranosylamine 
• 33758-19-9 N-bromoacetyl-β-D-glucopyranosylamine 
• 136860-06-5 N--L-phenylalanyl-L-leucyl>-β-D-glucopyranosylamine 
• 136863-94-0 N-(β-D-glucopyranosyl)-N'-(trans-2-iodocyclohexyl)urea 
• 134403-88-6 N-benzyloxycarbonyl-β-D-glucosylamine 
• 73847-68-4 β-D-glucopyranosyl-p-nitrophenyltriazene 
• 18918-51-9 N-(1-β-D-Glucopyranosyl)-4-nitro-benzamid 
• 15355-08-5 N-benzoyl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosylamine 
• 188849-84-5 (S)-2-Acetylamino-3-mercapto-3-methyl-N-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-butyramide 
• 50802-49-8 β-D-glucopyranosyl isothiocyanate 
• 288402-11-9 N-(β-D-glucopyranosyl)-N'-(p-methylphenyl)thiourea 
• 5513-36-0 2-amino>-2-deoxy-D-glucopyranose 
• 368886-89-9 (1,2-dideoxy-β-D-glucopyranoso)[1,2-d]-1,3-oxazolidine-2-thione 
• 76799-04-7 1-Benzyl-3-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-thiourea 

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.

Small molecule glycoconjugates with anticancer activity

Glycoconjugates are combinations of sugar moieties with organic compounds. Due to their biological resemblance, such structures often have properties that are desirable for drugs. In this study we designed and synthesised several glycoconjugates from smal

Preparation and evaluation of a molecular recognition bionic solid phase extraction column for separation of glucosides

Amolecular recognition bionic solid phase extraction (SPE) column for separation of glucosides has been prepared using a positively charged β-glucosylamidine as the ligand inwhich a glyconmoiety is connected via an N-glycoside linkage. β-Glucosylamidine, highly potent and selective inhibitors of β-glycosidase, is immobilized through a one-step synthesize procedure involving the addition of β-glucosylamine and 2-iminothiolane. HCl simultaneously to a matrix modified with maleimido groups via an appropriate spacer to give a molecular recognition absorbent for β-glucosides. N-octyl-β-D-glucopyranoside and β-D-galactopyranoside or α-D-mannopyranoside was directly chromatographed through the bionic chromatographic column, resulting in a much stronger retention of β-D-glucopyranoside than β-D-galactopyranoside and α-D-mannopyranoside. The retained glucopyranoside could only be eluted by glucose solution. This indicates that the binding of the glucoside was of specific nature that corresponds to the glycon substrate specificity of the glucoside. The ease of preparation and the selective nature of the molecular recognition bionic chromatography should promise a large-scale preparation of the molecular recognition adsorbent for the purification and removal of glucosides according to their glycon substrate specificity.