316555
1,6-Anhydro-β-D-glucose
99%
Sinônimo(s):
Levoglucosan
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About This Item
Fórmula empírica (Notação de Hill):
C6H10O5
Número CAS:
Peso molecular:
162.14
Beilstein:
80998
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
99%
Formulário
powder or crystals
atividade óptica
[α]18/D −66°, c = 1 in H2O
cor
beige
pf
182-184 °C (lit.)
solubilidade
water: 50 mg/mL, clear, colorless
cadeia de caracteres SMILES
O[C@H]1[C@H](O)[C@H]2CO[C@H](O2)[C@@H]1O
InChI
1S/C6H10O5/c7-3-2-1-10-6(11-2)5(9)4(3)8/h2-9H,1H2/t2-,3-,4+,5-,6-/m1/s1
chave InChI
TWNIBLMWSKIRAT-VFUOTHLCSA-N
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Aplicação
1,6-Anhydro-β-D-glucose (Levoglucosan) can be used as a precursor for the synthesis of:
- 1,6-anhydro-2,4-dideoxy-β-D-glycerohexopyranos-3-ulose.
- Quasi-linear polyglucose (PGlc) via cationic ring-opening polymerization.
- Polynitrogenated analogs of glucopyranoses.
- 3-deoxy-3-fluorogalactopyranose and acetylated 4-deoxy-4-fluorogalactopyranose.
Outras notas
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Chemosphere, 211, 617-623 (2018-08-11)
In the present study, a methodology involving hydrophilic interaction liquid chromatography (HILIC) and electrospray (ESI) tandem mass spectrometry (MS/MS) was developed for measurement of anhydrous monosaccharides as markers for wood burning in atmospheric aerosols, PM10. No extensive sample preparation, other
The controlled synthesis of polyglucose in one-dimensional coordination nanochannels
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Two classes of polar organic compounds, dicarboxylic acids (DCAs) and sugars/sugar anhydrides (S/SAs), were measured in airborne particulate matter in the area of Thessaloniki, northern Greece. The target compounds were measured simultaneously in two particle fractions PM10 and PM2.5 during
Practical synthesis of 1, 6-anhydro-2, 4-dideoxy-β -D-glycero-hexopyranos-3-ulose from levoglucosan
Belyk K, et al.
The Journal of Organic Chemistry, 65(8), 2588-2590 (2000)
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