468095-63-8

Basic information

• Product Name: 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE
• Synonyms: 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE;2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl p-TrifluoroMethylbenzylthio-N-(p-trifluoroMethylphenyl)forMiMidate;S-4-(Trifluoromethyl)benzyl O-((2R,3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl) (4-(trifluoromethyl)phenyl)carbonimidothioate;2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE
• CAS NO: 468095-63-8
• Molecular Formula: C50H45F6NO6S
• Molecular Weight: 901.95
• Product Categories: Biochemistry;Glucose;Glycosyl Donors;Imidate sugars;Sugars
• Mol File: 468095-63-8.mol
• Article Data: 0

Chemical Properties

• Melting Point: 120.0 to 125.0 °C
• Boiling Point: 843.5°C at 760 mmHg
• Flash Point: 464°C
• Appearance: /
• Density: 1.25g/cm³
• Vapor Pressure: 1.33E-27mmHg at 25°C
• Refractive Index: 1.564
• Storage Temp.: Freezer
• Solubility: slightly sol. in Chloroform
• PKA: -0.73±0.50(Predicted)
• CAS DataBase Reference: 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE(468095-63-8)
• EPA Substance Registry System: 2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE(468095-63-8)

Safety Data

• Hazardous Substances Data: 468095-63-8(Hazardous Substances Data)

Usage

Description

2,3,4,6-Tetra-O-benzyl-alpha-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate is a highly complex and specific compound containing a variety of chemical groups. It is a glucopyranosyl derivative with benzyl and trifluoromethyl groups, as well as a formimidate moiety.
Used in Organic Synthesis:
2,3,4,6-Tetra-O-benzyl-alpha-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate is used as a reagent for the formation of glycosidic bonds and in the preparation of glycosides. Its complex structure and specific reactivity make it a valuable tool for chemical and biological studies.
Used in Pharmaceutical Research:
2,3,4,6-Tetra-O-benzyl-alpha-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate is used as a reagent for modifying and selectively targeting specific molecules in biological and pharmaceutical research. Its functional groups make it particularly useful for these applications.
Used in Chemical Research:
2,3,4,6-Tetra-O-benzyl-alpha-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate is used as a reagent in chemical reactions, particularly in the formation of glycosidic bonds and in the preparation of glycosides. Its complex structure and specific reactivity make it a valuable tool for chemical and biological studies.

InChI:InChI=1/C50H45F6NO6S/c51-49(52,53)40-23-21-39(22-24-40)34-64-48(57-42-27-25-41(26-28-42)50(54,55)56)63-47-46(61-32-38-19-11-4-12-20-38)45(60-31-37-17-9-3-10-18-37)44(59-30-36-15-7-2-8-16-36)43(62-47)33-58-29-35-13-5-1-6-14-35/h1-28,43-47H,29-34H2/b57-48-/t43-,44-,45+,46-,47-/m1/s1