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Isopropylamine can be obtained by reaction of isopropyl alcohol with ammonia in presence of a catalyst: [3] (CH 3) 2 CHOH + NH 3 → (CH 3) 2 CHNH 2 + H 2 O. Isopropylamine is a building block for the preparation of many herbicides and pesticides including atrazine, bentazon, glyphosate, imazapyr, ametryne, desmetryn, prometryn, pramitol, dipropetryn, propazine, fenamiphos, and iprodione. [3]
Propylamine, also known as n-propylamine, is an amine with the chemical formula CH 3 (CH 2) 2 NH 2. [1] It is a colorless volatile liquid. [2] Propylamine is a weak base. Its K b (base dissociation constant) is 4.7 × 10 −4.
DIPEA is a sterically hindered organic base that is commonly employed as a proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, DIPEA has low solubility in water, which makes it very easily recovered in commercial processes, a combination of properties that makes it a useful organic reagent.
Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH 3) 2 CNH. It is a volatile and flammable liquid at room temperature . It is the simplest ketimine .
2-Amino-1-propanol, the hydrogenated derivative of alanine. 3-Amino-1-propanol, straight-chain and not widely used. 3-Amino-2-propanol (1-Aminopropan-2-ol) (isopropanolamines), prepared by addition of amines to one or two equivalents of propylene oxide. The propanolamines include many derivatives where the amine is secondary or tertiary.
Aminomethyl propanol (AMP) is an organic compound with the formula H 2 NC(CH 3) 2 CH 2 OH. It is colorless liquid that is classified as an alkanolamine. It is a useful buffer and a precursor to numerous other organic compounds. [2] Aminomethyl propanol is typically sold as a solution of the material in water, for which different concentrations ...
Diisopropylamine is a common amine nucleophile in organic synthesis. [4] Because it is bulky, it is a more selective nucleophile than other similar amines, such as dimethylamine. [5] It reacts with organolithium reagents to give lithium diisopropylamide (LDA). LDA is a strong, non-nucleophilic base [6]
1-Aminopropan-2-ol is the organic compound with the formula CH 3 CH(OH)CH 2 NH 2. It is an amino alcohol. The term isopropanolamine may also refer more generally to the additional homologs diisopropanolamine (DIPA) and triisopropanolamine (TIPA). 1-Aminopropan-2-ol is chiral. It can be prepared by the addition of aqueous ammonia to propylene ...