![]() Sodium 3-nitrobenzenesulfonate structure
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Common Name | Sodium 3-nitrobenzenesulfonate | ||
---|---|---|---|---|
CAS Number | 127-68-4 | Molecular Weight | 225.154 | |
Density | 1.637g/cm3 | Boiling Point | 215 - 219ºC | |
Molecular Formula | C6H4NNaO5S | Melting Point | 350 °C | |
MSDS | Chinese USA | Flash Point | 100 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Degradation of the synthetic dye amaranth by the fungus Bjerkandera adusta Dec 1: inference of the degradation pathway from an analysis of decolorized products.
Biodegradation 22(6) , 1239-45, (2011) 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 spectr... |
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Fabrication of biocompatible and tumor-targeting hyaluronan nanospheres by a modified desolvation method.
J. Pharm. Sci. 103(5) , 1529-37, (2014) The aim of this work was to maximize the tumor targetability of biocompatible hyaluronan (HA) by construction of a novel nanocarrier, using HA as the single material. HA was prefunctionalized with active amino groups, desolvated by acetone, and cross-linked b... |
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Discovery of a substituted 8-arylquinoline series of PDE4 inhibitors: structure-activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitor.
Bioorg. Med. Chem. Lett. 15(23) , 5241-6, (2005) 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 emesis... |
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Asymmetric cooperative catalysis of strong Brønsted acid-promoted reactions using chiral ureas.
Science 327(5968) , 986-90, (2010) 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 reac... |
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Kinetics of ozone reactions with 1-naphthalene, 1,5-naphthalene and 3-nitrobenzene sulphonic acids in aqueous solutions.
Water Sci. Technol. 44(5) , 7-13, (2001) 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... |
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