91274-05-4

Basic information

• Product Name: (2S,3S)-1,2-O-isopropylidene-1,2,3,4-tetrol
• Synonyms: (2S,3S)-1,2-O-isopropylidene-1,2,3,4-tetrol
• CAS NO: 91274-05-4
• Molecular Weight: 162.186
• Mol File: 91274-05-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S)-1,2-O-isopropylidene-1,2,3,4-tetrol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-1,2-O-isopropylidene-1,2,3,4-tetrol(91274-05-4)
• EPA Substance Registry System: (2S,3S)-1,2-O-isopropylidene-1,2,3,4-tetrol(91274-05-4)

Safety Data

• Hazardous Substances Data: 91274-05-4(Hazardous Substances Data)

Upstream product

• 120686-95-5 <4S-(R*,S*)>-α-Hydroxy-2,2-dimethyl-1,3-dioxolan-4-essigsaeure(phenylmethyl)ester 

Downstream Products

• 106757-57-7 (R,E)-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)prop-2-en-1-ol 
• 22323-80-4 (4S)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 14347-78-5 1,2-O-isopropylidene-D-glycerol 
• 93367-10-3 (2S,3S)-3,4-epoxy-1,2-di-O-isopropylidenebutane-1,2-diol 
• 36326-38-2 ethyl (E)-3-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]acrylate 
• 1310460-70-8 (1S)-2-(benzyloxy)-1-((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethan-1-ol 
• 111462-38-5 1-O-benzyl-3,4-O-isopropylidene-D-erythritol ⁽¹²⁾ and 2-O-benzyl-3,4-O-isopropylidene-D-erythritol 
• 1384244-51-2 C₁₆H₂₄O₄ 
• 1312135-98-0 (R)-4-benzyl-3-((R)-3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-methylpropanoyl)oxazolidin-2-one 
• 1312136-34-7 (R)-4-benzyl-3-(3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-propanoyl)oxazolidin-2-one 
• 106757-55-5 (E)-3-((R)-2,2-dimethyl[1,3]-dioxolan-4-yl)acrylic acid methyl ester 
• 106757-56-6 (Z)-(-)-methyl 3-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)acrylate 
• 146444-81-7 Benzoic acid (S)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(toluene-4-sulfonyloxy)-ethyl ester 
• 143884-06-4 (2S,3S)-10-acetoxy-1,2-O-isopropylidene-3-tert-butyldiphenylsiloxyundecane-1,2,3,10-tetraol 

Relevant articles and documents

Chiral Lactols, VIII - A Way for the Asymmetric Induction in the Formation of Sugars

The substituted glycol aldehyde 4 which bears an enantiomerically pure acetal-type protective group exhibiting the configuration of an α-L-sugar at the acetal centre is subjected to aldolization under basic conditions.The resulting products are reduced and characterized by comparison with reference compounds of known absolute configuration.L-Sugars are formed preferentially with L-erythrose being the main product.