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Merck
CN

316539

1,8-Naphthosultone

98%

Synonym(s):

1-Naphthol-8-sulfonic acid sultone, 8-Hydroxynaphthalene-1-sulfonic acid sultone

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About This Item

Empirical Formula (Hill Notation):
C10H6O3S
CAS Number:
83-31-8
Molecular Weight:
206.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24859025
EC Number:
201-468-0
Beilstein/REAXYS Number:
9381
MDL number:
MFCD00005937

Key Documents

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Product Name

1,8-Naphthosultone, 98%

InChI key

IEIADDVJUYQKAZ-UHFFFAOYSA-N

InChI

1S/C10H6O3S/c11-14(12)9-6-2-4-7-3-1-5-8(13-14)10(7)9/h1-6H

SMILES string

O=S1(=O)Oc2cccc3cccc1c23

assay

98%

form

solid

mp

154-157 °C (dec.) (lit.)

functional group

sulfonic acid

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315

Hazard Classifications

Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBV7862V
MKBN4649V
MKBB7102
MKBB0493
08512PH

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Sébastien Schmitt et al.
Chemical communications (Cambridge, England), 47(41), 11465-11467 (2011-09-29)
Sultones were subject to ring opening by nucleophilic attack with [(18)F]fluoride to afford easily purified (18)F-labelled hydrophilic sulfonated products in high yields. A two-step sequence including radiofluorination and coupling to lysine was then developed from a bis-sultone precursor as a
Sonia De Castro et al.
Journal of medicinal chemistry, 52(6), 1582-1591 (2009-02-20)
We report the synthesis and antiviral activity of a new family of non-nucleoside antivirals, derived from the 4-keto-1,2-oxathiole-2,2-dioxide (beta-keto-gamma-sultone) heterocyclic system. Several 4- and 5-substituted-5H-1,2-oxathiole-2,2-dioxide derivatives were found to have a selective inhibitory activity against human cytomegalovirus (HCMV) and varicella
A rationale for the selection of occlusion to induce and elicit delayed contact hypersensitivity in the guinea pig. A prospective test.
E V Buehler
Current problems in dermatology, 14, 39-58 (1985-01-01)
Single injection adjuvant test.
B F Goodwin et al.
Current problems in dermatology, 14, 201-207 (1985-01-01)
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
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