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An example of an ester formation is the substitution reaction between a carboxylic acid (R−C(=O)−OH) and an alcohol (R'OH), forming an ester (R−C(=O)−O−R'), where R and R′ are organyl groups, or H in the case of esters of formic acid.
2-Ethylhexanoic acid (2-EHA), commonly known as octoic acid, [2] is the organic compound with the formula CH 3 (CH 2) 3 CH(C 2 H 5)CO 2 H. It is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents.
An ester of a carboxylic acid.R stands for any group (typically hydrogen or organyl) and R ′ stands for any organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (R ′). [1]
Chromium(III) 2-ethylhexanoate: 3444-17-5 C 25 H 30 O 8: Kadsurin: 51670-40-7 C 25 H 36 O 6: Pseudopterosin A: 104855-20-1 C 26 H 32 N 6 O 11: Mirubactin: C 26 H 37 N 3 O Tarocin B: C 26 H 38 O 6: Pseudopterosin E: C 27 H 27 Cl 2 N 5 O 3 S JD5037: C 27 H 33 N 3 O 5: Andrimid: 108868-95-7 C 27 H 50 O 6: Axona: 538-23-8 C 28 H 26 ClN 5 O Basic ...
P. Potassium 2-ethylhexanoate; Potassium acetate; Potassium adipate; Potassium alum; Potassium aluminate; Potassium aluminium borate; Potassium aluminium fluoride
Chromium(III) 2-ethylhexanoate, C 24 H 45 CrO 6, is a coordination complex of chromium and ethylhexanoate. In combination with 2,5-dimethylpyrrole it forms the Phillips selective ethylene trimerisation catalyst [ 3 ] (not to be confused with Phillips catalyst ), used in the industrial production of linear alpha olefins , particularly 1-hexene ...