Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

316539

Sigma-Aldrich

1,8-Naphthosultone

98%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H6O3S
CAS Number:
Molecular Weight:
206.22
Beilstein/REAXYS Number:
9381
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

154-157 °C (dec.) (lit.)

functional group

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

InChI key

IEIADDVJUYQKAZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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)
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
Single injection adjuvant test.
B F Goodwin et al.
Current problems in dermatology, 14, 201-207 (1985-01-01)
DNA adducts of lactones, sultones, acylating agents and acrylic compounds.
J J Solomon
IARC scientific publications, (125)(125), 179-198 (1994-01-01)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service