62414-75-9

Basic information

• Product Name: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE
• Synonyms: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE;AITC;2,3,4-tri-o-acetyl-α-d-arabinopyranosyl isothiocyanate;2,3,4-tri-O-acetylarabinopyranosyl isothiocyanate
• CAS NO: 62414-75-9
• Molecular Formula: C₁₂H₁₅NO₇S
• Molecular Weight: 317.32
• Mol File: 62414-75-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 401.6°C at 760 mmHg
• Flash Point: 196.7°C
• Appearance: /
• Density: 1.4g/cm³
• Vapor Pressure: 1.17E-06mmHg at 25°C
• Refractive Index: 1.561
• Storage Temp.: −20°C
• BRN: 1690031
• CAS DataBase Reference: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE(62414-75-9)
• EPA Substance Registry System: 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE(62414-75-9)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-42
• Safety Statements: 23-26-36
• WGK Germany: 3
• F: 9
• Hazardous Substances Data: 62414-75-9(Hazardous Substances Data)

Usage

General Description

2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is a chemical compound with potential biological and pharmacological applications. It is a derivative of alpha-D-arabinopyranose and isothiocyanate, and features three acetyl groups attached to the sugar backbone. 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is known for its potential anticancer and antifungal properties, and has been the subject of research for its potential as a drug candidate. It may also have applications in the development of new pharmaceuticals and bioactive compounds. Further studies are needed to fully understand the potential benefits and applications of 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE.

InChI:InChI=1/C12H15NO7S/c1-6(14)18-9-4-17-12(13-5-21)11(20-8(3)16)10(9)19-7(2)15/h9-12H,4H2,1-3H3/t9-,10-,11+,12+/m1/s1

Upstream product

• 2290-65-5 trimethylsilyl isothiocyanate 
• 108646-05-5 (3S,4R,5R)-tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate 
• 39524-37-3 (2R,3S,4R,5R)-2-bromotetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 333-20-0 potassium thioacyanate 
• 113889-50-2 (3S,4R,5R)-2-bromotetrahydro-2H-pyran-3,4,5-triyl triacetate 

Downstream Products

• 73556-37-3 Acetic acid (2S,3S,4R,5R)-4,5-diacetoxy-2-(3-phenyl-5-thioxo-1,5-dihydro-[1,2,4]triazol-4-yl)-tetrahydro-pyran-3-yl ester 
• 77049-73-1 Acetic acid (2S,3S,4R,5R)-4,5-diacetoxy-2-(4-amino-2-thioxo-2H-[1,3,5]triazin-1-yl)-tetrahydro-pyran-3-yl ester 
• 73556-27-1 C₁₉H₂₃N₃O₈S 

Relevant articles and documents

A simple method for the preparation of glycosyl isothiocyanates

Glycosyl isothiocyanates became accessible from the corresponding peracetylated sugars in one step, by application of trimethylsilyl isothiocyanate and a Lewis acid in dichloromethane at room temperature. Georg Thieme Verlag Stuttgart.

STUDIES ON NUCLEOSIDE ANALOGS. XXIV. MONO- AND DISACCHARIDE ISOTHIOCYANATES

The reaction of mono- and disaccharide bromide with Pb(SCN)2 or AgSCN in dry benzene or benzene-toluene gives the respective mono- and disaccharide isothiocyanates and the confirmation of their stereochemistry of mono- and disaccharide isothiocyanates is