316539
1,8-萘磺酸内酯
98%
别名:
1-萘酚-8-磺酸内酯, 8-羟基萘-1-磺酸内酯
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关于此项目
经验公式（希尔记法）:
C10H6O3S
化学文摘社编号:
分子量:
206.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-468-0
Beilstein/REAXYS Number:
9381
MDL number:
Assay:
98%
Form:
solid
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
signalword
Warning
hcodes
Hazard Classifications
Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
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)
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
Natalia Paape et al.
Chemical communications (Cambridge, England), (33)(33), 3867-3869 (2008-08-30)
An efficient route to prepare ionic liquids with chloroalkylsulfonate anions is presented; the synthesis proceeds in a one-step ring-opening reaction of sultones with an organic chloride salt and provides a very attractive access to new anion functionalised ionic liquids.
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