151963-95-0

Basic information

• Product Name: N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL
• Synonyms: N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL;(2S,3R,4R,5S)-3,4,5-Tris(phenylMethoxy)-2-[(phenylMethoxy)Methyl]-1-(phenylMethyl)piperidine;N-Benzyl-2,3,4,6-tetra-O-benzyl-1-deoxy-L-idonojiriMycin
• CAS NO: 151963-95-0
• Molecular Formula: C41H43NO4
• Molecular Weight: 613.78442
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 151963-95-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 695.611°C at 760 mmHg
• Flash Point: 167.468°C
• Appearance: /
• Density: 1.183g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.633
• Storage Temp.: Refrigerator
• Solubility: Acetone (Slightly), Chloroform (Slightly), DMSO (Slightly)
• PKA: 7.61±0.10(Predicted)
• Stability: Moisture, Temperature Sensitive
• CAS DataBase Reference: N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL(CAS DataBase Reference)
• NIST Chemistry Reference: N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL(151963-95-0)
• EPA Substance Registry System: N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL(151963-95-0)

Safety Data

• Hazardous Substances Data: 151963-95-0(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Oil

InChI:InChI=1/C41H43NO4/c1-6-16-33(17-7-1)26-42-27-39(44-29-35-20-10-3-11-21-35)41(46-31-37-24-14-5-15-25-37)40(45-30-36-22-12-4-13-23-36)38(42)32-43-28-34-18-8-2-9-19-34/h1-25,38-41H,26-32H2/t38?,39-,40-,41?/m1/s1

Upstream product

• 100-39-0 benzyl bromide 
• 72458-46-9 N-benzyl-1-deoxynojirimycin 
• 100-46-9 benzylamine 
• 1316108-84-5 (2S,3R,4R,5R)-2,3,4,6-tetrakis(benzyloxy)-5-hydroxyhexyl pivalate 
• 1316108-89-0 (2R,3R,4R,5S)-1,3,4,5-tetrakis(benzyloxy)-6-(pivaloyloxy)hexan-2-yl benzoate 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 78136-16-0 2,3,4,6-tetra-O-benzyl-D-glucitol 
• 78136-16-0 (2S,3R,4R,5S)-2,3,4,6-tetrakis(benzyloxy)hexane-1,5-diol 
• 77638-00-7 2,3,4,6-tetra-O-benzyl-1,5-di-O-mesyl-D-glucitol 

Relevant articles and documents

Synthesis and activity towards yeast α-glucosidase of 1,5-dideoxy-1,5-imino-L-iditol (1-deoxy-L-idonojirimycin)

-

Facile and stereo-controlled synthesis of 2-deoxynojirimycin, Miglustat and Miglitol

A novel and facile synthesis of a series of the biologically significant iminosugar derivatives including 2-deoxynojirimycin, Miglustat and Miglitol is reported. The synthesis features a strategic double inversion mechanism for securing the desired stereochemistry at C5 position of such glucose-type carbohydrate mimetics, representing a practical and remarkable improvement on the previously reported method that suffers from the loss of the stereo-control during the reaction process. Crown Copyright