CAS 13639-54-8
:β-D-Glucopiranosio, 1-tio-, 2,3,4,6-tetraacetato 1-(O-etil carbonoditioato)
Descrizione:
β-D-Glucopiranosio, 1-tio-, 2,3,4,6-tetraacetato 1-(O-etil carbonoditioato) è un derivato del β-D-glucopiranosio, una forma ciclica a sei membri del glucosio. Questo composto presenta un legame tioetere nel carbonio anomerico, il che ne migliora la reattività e le potenziali applicazioni nella sintesi organica. La presenza di più gruppi acetile (tetraacetato) indica che i gruppi idrossilici sulla molecola di glucosio sono stati acetilati, il che può migliorare la solubilità e la stabilità del composto. Il gruppo O-etile carbonoditiato introduce gruppi funzionali aggiuntivi che possono partecipare a reazioni nucleofile, rendendo questo composto utile in varie trasformazioni chimiche. La sua struttura suggerisce che potrebbe mostrare attività biologiche specifiche, potenzialmente agendo come substrato o inibitore nei processi enzimatici. Come molti glicosidi e i loro derivati, le proprietà del composto, come solubilità, reattività e attività biologica, possono essere influenzate dall'acetilazione e dalle modifiche tioetere. In generale, questo composto rappresenta un glicoside complesso con potenziali applicazioni in chimica sintetica e biochimica.
Formula:C17H24O10S2
InChI:InChI=1S/C17H24O10S2/c1-6-22-17(28)29-16-15(26-11(5)21)14(25-10(4)20)13(24-9(3)19)12(27-16)7-23-8(2)18/h12-16H,6-7H2,1-5H3/t12-,13-,14+,15-,16+/m1/s1
InChI key:InChIKey=GYORARISFGRNMU-LJIZCISZSA-N
SMILES:O(C(C)=O)[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O[C@H]1SC(OCC)=S
Sinonimi:- 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthogenate
- 2,3,4,6-Tetra-O-acetyl-β-D-glucose ethylxanthat
- 2,3,4,6-tetra-O-acetyl-1-S-(ethoxycarbonothioyl)-1-thio-beta-D-glucopyranose
- 2,3,4,6-tetra-O-acetyl-1-S-(ethoxycarbothioyl)-1-thiohexopyranose
- Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(O-ethyl dithiocarbonate), β-<span class="text-smallcaps">D</span>-
- NSC 66060
- β-<span class="text-smallcaps">D</span>-Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(O-ethyl carbonodithioate)
- Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(O-ethyl dithiocarbonate), β-D-
- β-D-Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(O-ethyl carbonodithioate)
Ordinare per
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6 prodotti.
2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl Ethylxanthate
CAS:Formula:C17H24O10S2Colore e forma:SolidPeso molecolare:452.49652,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate-13C6
CAS:Prodotto controllato<p>Applications 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate-13C6 is an intermediate in synthesizing Aurothioglucose-13C6 (A794792), a labelled analogue of Aurothioglucose (A794790), which is used in the treatment of rheumatoid arthritis and psoriasis.<br>References Solomon, D. et al.: J. Am. Med. Assoc., 305, 2525 (2011); Madeira, J. et al.: Inflammopharm., 297, 20 (2012)<br></p>Formula:C11C6H24O10S2Colore e forma:NeatPeso molecolare:458.452,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate
CAS:Prodotto controllato<p>Applications 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Ethylxanthate (cas# 13639-54-8) is a compound useful in organic synthesis.<br></p>Formula:C17H24O10S2Colore e forma:NeatPeso molecolare:452.502,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl ethylxanthate
CAS:<p>2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl ethylxanthate is a synthetic carbohydrate that has been modified with acetyl groups. This modification is used to produce a carbohydrate that is more resistant to hydrolysis by enzymes. 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl ethylxanthate is one of many glycosides that have been modified with acetyl groups and fluorinated. This modification can be used for the synthesis of high purity carbohydrates.</p>Formula:C17H24O10S2Purezza:Min. 95%Colore e forma:White To Off-White SolidPeso molecolare:452.5 g/mol2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl ethylxanthate
CAS:<p>2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl ethylxanthate is an oligosaccharide that can be used as a building block for the synthesis of complex carbohydrates and glycosylation. It is synthesized by the reaction of 2,3,4,6-tetraacetylmannose with ethylxanthate in the presence of triethylamine. This compound is used for methylation reactions and click modification. It can also be used to modify saccharides and monosaccharides. The chemical formula of this compound is C14H24O8.</p>Formula:C17H24O10S2Purezza:Min. 95%Peso molecolare:452.5 g/mol



