43179-48-2

Basic information

• Product Name: L-ARABINOSE DIETHYLDITHIOACETAL
• Synonyms: L-ARABINOSE DIETHYLDITHIOACETAL;L-ARABINOSE DIETHYLTHIOACETAL;L-Arabinose-diethylmercaptal
• CAS NO: 43179-48-2
• Molecular Formula: C₉H₂₀O₄S₂
• Molecular Weight: 256.38
• Mol File: 43179-48-2.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 496.1±45.0 °C(Predicted)
• Appearance: /
• Density: 1.304±0.06 g/cm3(Predicted)
• PKA: 13.10±0.20(Predicted)
• CAS DataBase Reference: L-ARABINOSE DIETHYLDITHIOACETAL(CAS DataBase Reference)
• NIST Chemistry Reference: L-ARABINOSE DIETHYLDITHIOACETAL(43179-48-2)
• EPA Substance Registry System: L-ARABINOSE DIETHYLDITHIOACETAL(43179-48-2)

Safety Data

• Hazardous Substances Data: 43179-48-2(Hazardous Substances Data)

Upstream product

• 5328-37-0 L-arabinose 
• 75-08-1 ethanethiol 
• 532-20-7 L-arabinose 
• 38029-69-5 α-L-arabinofuranoside 
• 87-72-9 L-(+)-arabinose 

Downstream Products

• 10504-14-0 O²,O³;O⁴,O⁵-((Ξ,Ξ)-dibenzyliden)-L-arabinose-diethyldithioacetal 
• 196093-25-1 Thiobenzoic acid S-{(R)-2-[(4S,5R)-5-(bis-ethylsulfanyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-hydroxy-ethyl} ester 
• 196093-34-2 4-azido-5-S-benzoyl-4-deoxy-2,3-O-isopropylidene-5-thio-D-xylose 
• 91876-82-3 4-azido-5-O-benzoyl-4-deoxy-2,3-O-isopropylidene-D-xylose diethyl dithioacetal 
• 196093-30-8 Thiobenzoic acid S-{(S)-2-azido-2-[(4S,5R)-5-(bis-ethylsulfanyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester 
• 126448-14-4 5-O-p-toluenesulfonyl-2,3-O-isopropylidene-L-arabinose diethyl dithioacetal 
• 196093-24-0 5-O-benzoyl-4-O-methanesulfonyl-2,3-O-isopropylidene-L-arabinose diethyl dithioacetal 
• 196093-27-3 Thiobenzoic acid S-{(R)-2-[(4R,5R)-5-(bis-ethylsulfanyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-methanesulfonyloxy-ethyl} ester 
• 196093-26-2 Thiobenzoic acid S-[(R)-2-[(4R,5R)-5-(bis-ethylsulfanyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-(toluene-4-sulfonyloxy)-ethyl] ester 
• 196093-21-7 4,5-di-O-p-toluenesulfonyl-2,3-O-isopropylidene-L-arabinose diethyl dithioacetal 
• 74405-35-9 4,5-O-isopropylidene-L-arabinose di(ethylthio)acetal 
• 109734-77-2 O⁵-benzoyl-L-arabinose-phenylhydrazone 
• 35526-19-3 O²,O³,O⁴-Tribenzoyl-L-arabinose 
• 5115-88-8 2,3,4,5-tetra-O-acetyl-L-arabinose diethyl dithioacetal 

Relevant articles and documents

Synthesis of Anemoclemosides A and B, Two Saponins Isolated from Anemoclema glaucifolium

Steroidal and triterpenoid saponins are attractive for their wide-ranging pharmacological properties. The triterpenoid saponins Anemoclemoside A and B are root constituents of the Chinese folk medicinal plant Anemoclema glaucifolium (Ranunculaceae). Both

The first convergent total synthesis of penarolide sulfate A2, a novel α-glucosidase inhibitor

Penarolide sulfate A2, a 31-membered macrolide encompassing a proline residue and three sulfate groups, was firstly synthesized in 16 linear steps with 4.8% overall yield. Three consecutive stereogenic centers in penarolide sulfate A2 were efficiently derived from natural chiral template l-arabinose. The crucial assembly reactions included Brown asymmetric allylation, olefin cross-metathesis, alkyne-epoxide coupling, and macrolactamization. The anti-yeast α-glucosidase activities of penarolide sulfate A2 and its fully desulfated derivative were examined showing IC50 values of 4.87 and 10.74 μg mL-1, respectively.

Synthesis of substituted imidazolo[1,2-α]piperidinoses and their evaluation as glycosidase inhibitors

The synthesis of substituted imidazolo[1,2-α]-L-arabino-piperidinoses is reported. The substituents are methyl, phenylmethyl, phenylethyl, cyclohexylethyl, pyridinylethyl, piperidinylethyl, phenylpropyl and hydroxymethyl. All substituents are connected to