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316539

1,8-Naphthosultone

Name: 1,8-Naphthosultone
Brand: ALDRICH

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

Assay:

98%

Form:

solid

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Properties

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

Description

pictograms

GHS07

signalword

Warning

hcodes

H315

pcodes

P264 - P280 - P302 + P352 - P332 + P313 - P362 + P364

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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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)

DNA adducts of lactones, sultones, acylating agents and acrylic compounds.

J J Solomon

IARC scientific publications, (125)(125), 179-198 (1994-01-01)

Isolation of a sultone as an unusual acetolysis product.

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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Global Trade Item Number

SKU	GTIN
316539-25G	04061833021422