155417-88-2

Basic information

• Product Name: 2-O-benzyl-erythrobutanetetrol
• Synonyms: 2-O-benzyl-erythrobutanetetrol
• CAS NO: 155417-88-2
• Molecular Weight: 212.246
• Mol File: 155417-88-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-O-benzyl-erythrobutanetetrol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-benzyl-erythrobutanetetrol(155417-88-2)
• EPA Substance Registry System: 2-O-benzyl-erythrobutanetetrol(155417-88-2)

Safety Data

• Hazardous Substances Data: 155417-88-2(Hazardous Substances Data)

Upstream product

• 1259016-42-6 1,3-O-benzylidene-2-O-benzyl-L-erythritol 
• 131543-46-9 Glyoxal 
• 60656-87-3 benzyloxyacetoaldehyde 
• 169738-13-0 2,3-O-(R)-benzylidene-D-erythronolactone 
• 91143-55-4 3-O-benzyl-D-erythronolactone 
• 21066-72-8 diethyl tartrate 
• 100-52-7 benzaldehyde 

Downstream Products

• 104322-67-0 (R)-2-Benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethanol 
• 155301-42-1 Benzoic acid (R)-2-benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl ester 
• 155301-43-2 Benzoic acid (2R,3S)-2-benzyloxy-3,4-dihydroxy-butyl ester 

Relevant articles and documents

Asymmetric aldol reaction of glyoxal catalyzed by diarylprolinol

All selection should be this- eeasy: The direct asymmetric aldol reaction of commercial aqueous glyoxal is catalyzed by trifluoromethyl-substituted diarylprolinol 1 to afford a β-formyl-β-hydroxy-α-substituted aldehyde in good yield with excellent anti selectivity and excellent enantioselectivity.

A Straightforward Preparation of Both Enantiomerically Pure 2-O-Benzyl-erythro-Butanetetrols

A short and efficient synthesis of both enatiomerically pure 2-O-benzyl-erythro-butanetetrols 4 and ent-4 from the readily available D-erthronolactone 1 is presented.The synthesis proceeds in a highly efficient manner and is in both cases substrate controlled.