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The latter process provides a high-yield route to 1,1-binaphthol: [22] Such compounds are intermediates in the synthesis of BINAP and its derivatives. [20] Copper(II) chloride dihydrate promotes the hydrolysis of acetonides, i.e., for deprotection to regenerate diols [23] or aminoalcohols, as in this example (where TBDPS = tert ...
Chemical formula Synonyms CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA): 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0
IR absorption spectrum of copper(I) chloride. Copper(I) chloride, commonly called cuprous chloride, is the lower chloride of copper, with the formula CuCl.The substance is a white solid sparingly soluble in water, but very soluble in concentrated hydrochloric acid.
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
Like other complexing agents in the aminopolycarboxylic acid class, trisodium N-(1-carboxylatoethyl)iminodiacetate (α-ADA) finds due to its ability to form stable chelate complexes with polyvalent ions (in particular the water hardening agents Ca 2+ and Mg 2+, as well as transition and heavy metal ions such as Fe 3+, Mn 2+, Cu 2+, etc.) use in ...
Copper(II) acetate, also referred to as cupric acetate, is the chemical compound with the formula Cu(OAc) 2 where AcO − is acetate (CH 3 CO − 2).The hydrated derivative, Cu 2 (OAc) 4 (H 2 O) 2, which contains one molecule of water for each copper atom, is available commercially.
Calcium chloride was apparently discovered in the 15th century but wasn't studied properly until the 18th century. [11] It was historically called "fixed sal ammoniac" (Latin: sal ammoniacum fixum [12]) because it was synthesized during the distillation of ammonium chloride with lime and was nonvolatile (while the former appeared to sublime); in more modern times (18th-19th cc.) it was called ...
The compound is synthesized by the reaction of cobalt(II) chloride and ethylenediamine in hydrochloric acid in the presence of oxygen: . 4 CoCl 2 + 8 en + 4 HCl + O 2 → 4 trans-[CoCl 2 (en) 2]Cl + 2 H 2 O
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