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The general structure of a boronic acid, where R is a substituent. A boronic acid is an organic compound related to boric acid (B(OH) 3) in which one of the three hydroxyl groups (−OH) is replaced by an alkyl or aryl group (represented by R in the general formula R−B(OH) 2). [1]
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]
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
2-Chloropyridine is an aryl chloride with the formula C 5 H 4 ClN. It is a colorless liquid that is mainly used to generate fungicides and insecticides in industry. It also serves to generate antihistamines and antiarrythymics for pharmaceutical purposes. [2] It is one of three isomers of chloropyridine.
The terms polymer and macromolecule do not mean the same thing. A polymer is a substance composed of macromolecules. The latter usually have a range of molar masses (unit g mol −1), the distributions of which are indicated by dispersity (Đ).
3-Methylpyridine or 3-picoline, is an organic compound with formula 3-CH 3 C 5 H 4 N. It is one of three positional isomers of methylpyridine, whose structures vary according to where the methyl group is attached around the pyridine ring. This colorless liquid is a precursor to pyridine derivatives that have applications in the pharmaceutical ...
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 .
C 6 H 5 NO 2: picolinic acid: 98-98-6 C 6 H 5 NO 3: 4-nitrophenol: 100-02-7 6-hydroxyniacin: 5006-66-6 C 6 H 5 OH: phenol: 108-95-2 C 6 H 5 O 7 3−: citrate ion: 126-44-3 C 6 H 5 NO 4: Citrazinic acid: 99-11-6 (C 6 H 5) 4 Ge: tetraphenylgermane: 1048-05-1 (C 6 H 5) 2 O: diphenyl ether: 101-84-8 (C 6 H 5) 3 N: triphenylamine: 603-34-9 (C 6 H 5 ...