1229900-82-6

Basic information

• Product Name: (4S,5RS,6R)-2-(acetoxymethyl)-6-(3-((R)-2-(dimethylamino)-1-phenylethyl)thioureido)tetrahydro-2H-pyran-3,4,5-triyl triacetate
• Synonyms: (4S,5RS,6R)-2-(acetoxymethyl)-6-(3-((R)-2-(dimethylamino)-1-phenylethyl)thioureido)tetrahydro-2H-pyran-3,4,5-triyl triacetate
• CAS NO: 1229900-82-6
• Molecular Weight: 553.634
• Mol File: 1229900-82-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5RS,6R)-2-(acetoxymethyl)-6-(3-((R)-2-(dimethylamino)-1-phenylethyl)thioureido)tetrahydro-2H-pyran-3,4,5-triyl triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5RS,6R)-2-(acetoxymethyl)-6-(3-((R)-2-(dimethylamino)-1-phenylethyl)thioureido)tetrahydro-2H-pyran-3,4,5-triyl triacetate(1229900-82-6)
• EPA Substance Registry System: (4S,5RS,6R)-2-(acetoxymethyl)-6-(3-((R)-2-(dimethylamino)-1-phenylethyl)thioureido)tetrahydro-2H-pyran-3,4,5-triyl triacetate(1229900-82-6)

Safety Data

• Hazardous Substances Data: 1229900-82-6(Hazardous Substances Data)

Upstream product

• 14152-97-7 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate 
• 174636-94-3 (R)-N²,N²-dimethyl-1-phenyl-1,2-ethanediamine 

Relevant articles and documents

Doubly stereocontrolled asymmetric conjugate addition of acetylacetone to nitroolefins catalyzed by bifunctional tertiary amine-thiourea catalysts derived from both acyclic α-amino acids and carbohydrates

A novel class of easily preparative, cheap, and fine-tunable bifunctional chiral tertiary amine-thiourea organocatalysts have been developed by combining both acyclic diamines derived from acyclic α-amino acids and carbohydrates. These organocatalysts pro