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Sigma-Aldrich

Natrium-3-nitrobenzolsulfonat Natriumsalz

98%

Synonym(e):

Natrium-3-nitrobenzolsulfonat

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About This Item

Lineare Formel:
O2NC6H4SO3Na
CAS-Nummer:
127-68-4
Molekulargewicht:
225.15
Beilstein:
3639982
EG-Nummer:
204-857-3
MDL-Nummer:
MFCD00007490
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24853484
NACRES:
NA.22

Assay

98%

Löslichkeit

water: 50 mg/mL, clear to slightly hazy, faintly yellow to yellow

SMILES String

[Na+].[O-][N+](=O)c1cccc(c1)S([O-])(=O)=O

InChI

1S/C6H5NO5S.Na/c8-7(9)5-2-1-3-6(4-5)13(10,11)12;/h1-4H,(H,10,11,12);/q;+1/p-1

InChIKey

LJRGBERXYNQPJI-UHFFFAOYSA-M

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Anwendung

Sodium 3-nitrobenzenesulfonate (3-Nitrobenzenesulfonic acid sodium salt) was used in the synthesis of quinoline.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H317,H319

Gefahreneinstufungen

Eye Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

212.0 °F - closed cup

Flammpunkt (°C)

100 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Analysenzertifikate (COA)

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Natriumdodecylbenzolsulfonat technical grade

Sigma-Aldrich

289957

Natriumdodecylbenzolsulfonat

Trifluoressigsäure ReagentPlus®, 99%

Sigma-Aldrich

T6508

Trifluoressigsäure

Dichlormethan anhydrous, ≥99.8%, contains 40-150 ppm amylene as stabilizer

Sigma-Aldrich

270997

Dichlormethan

Jay P Kitt et al.
Journal of the American Chemical Society, 139(10), 3851-3860 (2017-02-22)
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This paper describes the ozone oxidation kinetics of 1-naphthalene (1 NS), 1,5-naphthalene (1,5NDS), and 3-nitrobenzene (3NBS) sulphonic acid. The presence of hydroxyl radicals and their effect on the overall rate of reaction was studied. Second order kinetic constants of direct
Hao Xu et al.
Science (New York, N.Y.), 327(5968), 986-990 (2010-02-20)
Cationic organic intermediates participate in a wide variety of useful synthetic transformations, but their high reactivity can render selectivity in competing pathways difficult to control. Here, we describe a strategy for inducing enantioselectivity in reactions of protio-iminium ions, wherein a
Dwight Macdonald et al.
Bioorganic & medicinal chemistry letters, 15(23), 5241-5246 (2005-09-20)
The discovery and SAR of a new series of substituted 8-arylquinoline PDE4 inhibitors are herein described. This work has led to the identification of several compounds with excellent in vitro and in vivo profiles, including a good therapeutic window of
Nichina Gomi et al.
Biodegradation, 22(6), 1239-1245 (2011-04-29)
We examined the degradation of amaranth, a representative azo dye, by Bjerkandera adusta Dec 1. The degradation products were analyzed by high performance liquid chromatography (HPLC), visible absorbance, and electrospray ionization time-of-flight mass spectroscopy (ESI-TOF-MS). At the primary culture stage
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