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Wichtige Dokumente
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1,8-Naphthosulton
98%
Synonym(e):
1-Naphthol-8-sulfonsäuresulton
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About This Item
Empirische Formel (Hill-System):
C10H6O3S
CAS-Nummer:
Molekulargewicht:
206.22
Beilstein:
9381
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Assay
98%
Form
solid
mp (Schmelzpunkt)
154-157 °C (dec.) (lit.)
Funktionelle Gruppe
sulfonic acid
SMILES String
O=S1(=O)Oc2cccc3cccc1c23
InChI
1S/C10H6O3S/c11-14(12)9-6-2-4-7-3-1-5-8(13-14)10(7)9/h1-6H
InChIKey
IEIADDVJUYQKAZ-UHFFFAOYSA-N
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Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Skin Irrit. 2
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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DNA adducts of lactones, sultones, acylating agents and acrylic compounds.
J J Solomon
IARC scientific publications, (125)(125), 179-198 (1994-01-01)
The derivation of quantitative correlations between skin sensitisation and physio-chemical parameters for alkylating agents, and their application to experimental data for sultones.
D W Roberts et al.
Journal of theoretical biology, 99(4), 807-825 (1982-12-21)
Scott A Wolckenhauer et al.
Organic letters, 9(21), 4363-4366 (2007-09-25)
Rhodium-catalyzed reactions of sulfonate ester derivatives are biased strongly toward 1,6-insertion and thus offer a general method for assembling delta-sultones. Two protocols for staging this cyclization reaction are described, which capitalize on the unique ability of either diazo or iodonium
Donald C Craig et al.
Carbohydrate research, 346(6), 854-857 (2011-03-11)
Acetolysis of methyl 5,6-di-O-acetyl-2,3-O-isopropylidene-β-L-gulofuranoside has yielded a sultone, 4-(1,2,5,6-tetra-O-acetyl-β-L-gulofuranos-3-yl)-6-methyl-1,2-oxathiin 2,2-dioxide (2) whose structure was determined by X-ray diffraction. (1)H and (13)C NMR spectral properties of 2 are presented together with a rationale for its formation. Preparation and properties of the
Thomas Priem et al.
Organic & biomolecular chemistry, 10(5), 1068-1078 (2011-12-14)
A novel homobifunctional cross-linker based on a bis-sultone benzenic scaffold was synthesised. The potential utility of this bioconjugation reagent was demonstrated through the preparation of an original prosthetic group suitable for the [(18)F]-labelling of peptides. The labelling strategy is based
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