Ad
related to: 4 formylbenzoic acid another name for potassium nitrate 5 mg
Search results
Results From The WOW.Com Content Network
4-Carboxybenzaldehyde (CBA) is an organic compound with the formula OCHC 6 H 4 CO 2 H. It consists of a benzene ring substituted with both an aldehyde and a carboxylic acid, with these functional groups on opposite corners of the ring. This compound is formed in 0.5% yield as a byproduct in the production terephthalic acid from p-xylene. Since ...
KC 4 H 5 O 6: potassium bitartrate: 868–14–4 KC 7 H 5 O 2: potassium benzoate: 582–25–2 KCl: potassium chloride: 7447–40–7 KClO 3: potassium chlorate: 3811–04–9 KClO 4: potassium perchlorate: 7778–74–7 K 2 CuCl 4: potassium tetrachlorocuprate: 13877–24–2 KF: potassium fluoride: 7789–23–3 KH: potassium hydride: 7693 ...
Potassium nitrate can be made by combining ammonium nitrate and potassium hydroxide. NH 4 NO 3 + KOH → NH 3 + KNO 3 + H 2 O. An alternative way of producing potassium nitrate without a by-product of ammonia is to combine ammonium nitrate, found in instant ice packs, [30] and potassium chloride, easily obtained as a sodium-free salt substitute.
C 6 H 4 BrNO 2: 5-bromonicotinic acid: 20826-04-4 C 6 H 4 ClNO 2: 2-chloronicotinic acid: 2942-59-8 C 6 H 4 ClN 3: 4-Chlorophenyl azide: C 6 H 4 ClNO 2: 6-chloro-2-pyridinecarboxylic acid: 4684-94-0 6-chloronicotinic acid: 5326-23-8 C 6 H 4 N 4: tricyanoaminopropene: C 6 H 4 O 2: orthobenzoquinone: 583-63-1 parabenzoquinone quinone: 106-51-4 C ...
Dehydration by means of strong acid gives 3-Butylisocarbostyril [132-90-1] (8). Phosphorus oxychloride converts the oxygen function to the corresponding chloride via the enol forms 3-butyl-1-chloroisoquinoline [87-06-9] (9). Displacement of halogen with the sodium salt from 2-dimethylaminoethanol (10) affords dimethisoquin (11).
4-Formylphenyl boronic acid crystallizes in colorless needles [1] or is obtained as an odorless, whitish powder, which dissolves little in cold but better in hot water. The compound is quite stable [3] and readily forms dimers and cyclic trimeric anhydrides, which complicate purification and tend to protodeboronize, a secondary reaction that occurs frequently in the Suzuki coupling, with ...
Benzoic acid and its salts are used as food preservatives, represented by the E numbers E210, E211, E212, and E213. Benzoic acid inhibits the growth of mold, yeast [23] and some bacteria. It is either added directly or created from reactions with its sodium, potassium, or calcium salt. The mechanism starts with the absorption of benzoic acid ...
It also can be prepared by treating benzaldehyde under nitration conditions, a process that initially converts the aldehyde to the acid. 4-Nitrobenzoic acid is a precursor to 4-aminobenzoic acid , which is in turn used to prepare the anesthetic procaine . 4-Nitrobenzoic acid is prepared by oxidation of 4-nitrotoluene .