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2,6-Dichloropyridine is a chloropyridine with the formula C 5 H 3 Cl 2 N. A white solid, it is one of six isomers of dichloropyridine . It serves as a precursor to the antibiotic enoxacin , [ 2 ] as well as the drug and anpirtoline and the antifungal liranaftate .
Dichloropyridines are organic compounds with the formula Cl 2 C 5 H 3 N, consisting of a pyridine ring substituted with two chlorides. [1] Six isomers are known. They are white or colorless, most are solids at room temperature.
In these conversions, chloride is displaced. [2] Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. Oxidation 2-chloropyridine gives 2-chloropyridine-N-oxide. [5] The antihistamine pheniramine may be generated via the reaction of phenylacetonitrile with 2-chloropyridine in the presence of a base ...
Direct halogenation of pyridine with chlorine gas above 270 °C gives a mixture of 2-chloropyridine and 2,6-dichloropyridine. [1] 2- and 4-chloropyridine are prepared from the corresponding pyridinols using phosphoryl chloride. [1]
An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.
Clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) is a selective herbicide used for control of broadleaf weeds, especially thistles and clovers.Clopyralid is in the picolinic acid family of herbicides, which also includes aminopyralid, picloram, triclopyr, and several less common herbicides.
51% (C 3 S), 24% (C 2 S), 6% (C 3 A), 11% (C 4 AF), 2.9% MgO, 2.5% (SO 3), 0.8% ignition loss, and 1.0% free CaO. A limitation on the composition is that the (C 3 A) shall not exceed 8%, which reduces its vulnerability to sulphates. This type is for general construction exposed to moderate sulphate attack, and is meant for use when concrete is ...
H 2 SO 4 + Ca(OH) 2 → CaSO 4 · 2H 2 O. When concrete also contains limestone aggregates or a filler addition, H 2 SO 4 reacts with calcite (CaCO 3) and water to also form gypsum while releasing CO 2: H 2 SO 4 + CaCO 3 + H 2 O → CaSO 4 · 2H 2 O + CO 2. Gypsum is relatively soluble in water (~ 1 – 2 g/L), so there is plenty of calcium and ...