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2-Nitrophenylacetic acid is an organic compound used in organic synthesis that has also been used as an herbicide. It is a derivative of phenylacetic acid , containing a phenyl functional group , a carboxylic acid functional group, and a nitro functional group.
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
Chloroformic acid (ClCO 2 H) 0.27 [5] Acetic acid (CH 3 CO 2 H) 4.76 Glycine (NH 2 CH 2 CO 2 H) 2.34 Fluoroacetic acid (FCH 2 CO 2 H) 2.586 Difluoroacetic acid (F 2 CHCO 2 H) 1.33 Trifluoroacetic acid (CF 3 CO 2 H) 0.23 Chloroacetic acid (ClCH 2 CO 2 H) 2.86 Dichloroacetic acid (Cl 2 CHCO 2 H) 1.29 Trichloroacetic acid (CCl 3 CO 2 H) 0.65 ...
A pyridinecarboxylic acid is any member of a group of organic compounds which are monocarboxylic derivatives of pyridine. Pyridinecarboxylic acid comes in three isomers: Picolinic acid (2-pyridinecarboxylic acid) Nicotinic acid (3-pyridinecarboxylic acid), also known as Niacin; Isonicotinic acid (4-pyridinecarboxylic acid)
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2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula Cl 2 C 6 H 3 OCH 2 CO 2 H.It is usually referred to by its ISO common name 2,4-D. [4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.
This reaction is rapid and stoichiometric, with the addition of one mole of thiol releasing one mole of TNB. The TNB 2− is quantified in a spectrophotometer by measuring the absorbance of visible light at 412 nm, using an extinction coefficient of 14,150 M −1 cm −1 for dilute buffer solutions, [4] [5] and a coefficient of 13,700 M −1 cm −1 for high salt concentrations, such as 6 M ...
n HO−CR 2 −X−CR 2 −OH + n COCl 2 → [−O−CR 2 −X−CR 2 −O−C(=O)−] n + 2n HCl. An example is the reaction of phosgene with bisphenol A to form polycarbonates. [9] Phosgenation of diamines gives di-isocyanates, like toluene diisocyanate (TDI), methylene diphenyl diisocyanate (MDI), hexamethylene diisocyanate (HDI), and ...