Cupric acetate, basic

Synonyms cupric acetate, basic cupric subacetate... 

Cupric Acetate, Basic, Cupric subacetatc. Several... 

The cupric acetate-pyridine reagent provides a homogenous and basic reaction medium. The yields are high, and there is seldom precipitation of the cuprous derivative which may slow down the cuprous chloride-oxygen procedure. ... 

A basic copper chlorate is formed when soln. of potassium chlorate acidified with sulphuric acid are electrolyzed with an alternating current between copper electrodes (L. Rossi) 83 when the hydrate is heated above 100° (A. Wachter) when a soln. of copper chlorate be mixed with pieces of marble or urea, and heated in a sealed tube to 130° (L. Bourgeois) when the hydroxides of the alkalies or alkaline earths act on cupric chlorate soln., or copper hydroxide acts on soln. of potassium chlorate (A. Brochet) when hydrated cupric oxide or cupric hydroxide acts on cupric chlorate soln. (P. Sabatier) or when potassium chlorate acts on cupric acetate soln. (A. Casselmann), basic cupric chlorate is obtained. The basic chlorate forms bluish-green monoclinic prisms of sp. gr. 3 55 and composition 4Cu0.C1205.3H20, that is, Cu(C103)2.3Cu(0H)2, which A. Werner considers to be hexahydroxyl cupric chlorate ... 

Conceptually, assays for lipase activity using the colorimetric method (copper-soap procedure Basic Protocol 2) are similar to titrimetry in that liberated fatty acids are being measured however, the colorimetric method is more specific for fatty acids (Lowry and Tinsley, 1976). Quenched subsamples of emulsified acylglycerol/lipase reaction mixtures are combined with the biphasic mixture of cupric acetate/pyridine and benzene. Cupric salts of the fatty acids are formed (molar stoichiometry of fatty acid to Cu2+ of 4 2) and these soaps, which are blue in color, are partitioned into benzene to allow for quantification by measuring absorbance of the clear benzene phase at 715 nm. 

Aldehydes have been formed from alcohols by the use of other oxidizing agents. Dihydroxyacetone has been oxidized with excess cupric acetate to hydroxypyruvic aldehyde in 87% yield. p-Cyanobenzyl alcohol treated at 0° with a chloroform solution of nitrogen tetroxide gives practically pure p-cyanobenzaldehyde (90%). Aromatic alcohols containing nitro groups have been oxidized to the corresponding nitro aldehydes with concentrated nitric acid, e.g., o- and p-nitrobenzaldehydes (80-85%). m-Nitrobenzenesulfonic acid in basic media has been used for the oxidation of substituted benzyl alcohols, most satisfactorily for the water-soluble phenolic benzyl alcohols. Selenium dioxide, or less effectively tellurium dioxide, oxidizes benzyl alcohol slowly to benzaldehyde. ... 

K bromate 0,7, K (or Na) chlorate 0.5 to l.O sulfur (or charcoal) 0.5 to 0.8 part. Deflagration of this compn produced abundant violet-grey smoke-Cupric Acetate, Cu(CgH302)2 H O grn-blue pdr decompg beginning at 240° can be prepd by the action of AcOH on CuO or by other methods (Ref. 2). The cupric salt can serve as a basic material in the prepn of Cu(II) aceto-arsenite, an ingredient of some pyrotechnic compns. The so-called Ruggieri s Russian Fire compn contained Cu acetate 4, Cu sulfate 2 ... 

CUPRIC ACETATE or CUPRIC ACETATE MONOHYDRATE (142-71-2) Cu(C2H30j)2 H20 Noncoiribustible solid. Solution in water is basic reacts with acids. Incompatible with acetylides, hydrazine,... 

COUMARILIC ACID, 24, 33 Coumarin, 24, 33 Coumarin dibromide, 24, 33 Coumarin, 4-methyl-, 24, 69 Coupling, of allyl chloride, 27, 7 of aryl residues, 20, 45 Crab shells, 26, 36 Creatinine, 22, 90 /i-Cresol, 2-bromo-, 23,11 Crotonaldehyde, 24, 92 27, 66 Crotonic acid, SO, 101 24, 98 26, 55 Crotonio acid, /3-anilino-, ethyl ESTER, 29, 42 Cupric acetate, 28, 45 Cupric carbonate, basic, 24, 64 Cupro-cupri sulfite, 28, 53 Cuprous bromide, 24, 22, 23 Cuprous chloride, 28, 46 Cuprous cyanide, 21, 89 24, 14, 97 28, 34... 

Xie and co-workers reported the N-arylation of imidazole in refluxing methanol in the presence of catalytic cuprous chloride or cupric acetate in air [26]. Yields are higher than the catalytic [Cu(OH) TM EDA 2C]l2 condition first introduced by Collman and co-workers [33a, b]. Similarly, the same conditions are applicable to phfhalamides [26], also with better yields than previously reported by Lam and co-workers [33c], Conversely, for aniline and sulfonamide substrates, Xie s conditions gave lower yield than Lam s conditions [33c]. Likewise, for basic amines, Batey s conditions [27] are superior. 

BASF see Badische aniline-und sodafabrik 2 B4 Bashforth chronograph see Chronographs 3 C308 Basic cupric azide 1 A533 Basic lead acetate 1 A28 Basic lead azide 1 A555... 

A Wacker catalyst is used in this process, similar to that for the manufacture of acetic acid. Since the acetic acid can also be made from ethylene, the basic raw material is solely ethylene. A liquid-phase process has been replaced by a vapor-phase reaction run at 70 to 140 psi and 175 to 200°C. Catalysts may be (1) carbon-palladium chloride-cupric chloride (C-PdCl2-CuCl2), (2) palladium chloride-alumina (PdCl2-Al203), or (3) palladium-carbon-potassium acetate (Pd-C-KOAc). The product is distilled into water, acetaldehyde that can be recycled to acetic acid, and the pure colorless liquid, which is collected at 72°C. The yield is 95percent. 

Inorganic copper compounds include cuprous oxide cupric oxide copper hydroxide copper carbonate basic copper ammonium carbonate copper acetate copper sulfate copper sulfate, tribasic (Bordeau Mixture) copper oxychloride copper silicate copper lime dust and copper potassium sulfide. Figure 5.10 shows a package of Kocide 101, copper containing products. 

N-Acetylation of basic amino acids. The reagent reacts with an aqueous solution of the copper salt of a basic amino acid to give the N-acetyl derivative.1 The procedure is superior to the usual synthesis in which acetic anhydride is used because the reaction goes to completion. As applied to L-lysine, the method is simple and gives better yields of pure e-N-acetyl-L-lysine. Excess cupric carbonate is added to a boiling aqueous solution of L-lysine (0.1 mole) and the solution is filtered and cooled to 25° and treated with sodium bicarbonate, p-nitrophenylacetate, and a few milliliters of ethyl acetate to keep the acetate in solution. After stirring for 15 hrs the copper salt which separates is filtered, suspended in water, and freed of copper with H2S. The solution is evaporated to dryness and the N-acetyllysine crystallized from water-ethanol. 

ACETIC ACID, COBALT(II) SALT (71-48-7) Co(CjH30j)i 4HOH Noncombustible solid. Solution in water is basic (pH 6.8 to >7.0) reacts with acids. Some cobalt compounds react with oxidizers, acetylene. Cobalt is a known animal carcinogen. ACETIC ACID, CUPRIC SALT (142-71-2) Cu(C2H302)i H20 Noncombustible solid. Solution in water is basic reacts with acids. Incompatible with acetylides, hydrazine, nitromethane, mercurous chloride nitrates, sodium hypobromite. Thermal decomposition releases fumes of copper, acetic acid, and carbon oxides. 

---