tertiary butyl alcohol
41stain — 1. To discolor. 2. To color; to dye. 3. A discoloration. 4. A dye used in histologic and bacteriologic technique. 5. A procedure in which a dye or combination of dyes and reagents is used to color the constituents of cells and tissues. For… …
42Dicycloverine — Systematic (IUPAC) name 2 (diethylamino)ethyl bi(cyclohexane) 1 carboxylate Clinical data Trade names Byclomi …
43Clomipramine — Systematic (IUPAC) name 3 (3 chloro 10,11 dihydro 5H dibenzo[b,f]azepin 5 yl) N,N dimethylpropan 1 amine Clinical data Trade names …
44Boronic acid — The general structure of a boronic acid, where R is a substituent. A boronic acid is an alkyl or aryl substituted boric acid containing a carbon–boron bond belonging to the larger class of organoboranes. Boronic acids act as Lewis acids. Their… …
45Criegee rearrangement — The Criegee rearrangement is a rearrangement reaction named after Rudolf Criegee. In this organic reaction a tertiary alcohol is cleaved in an organic oxidation by a peroxyacid to a ketone. The acid used is often p nitroperoxybenzoic acid because …
46Arylcyclohexylamine — Phencyclidine, the prototypal arylcyclohexylamine derivative. Arylcyclohexylamines, also known as arylcyclohexamines or arylcyclohexanamines, are a chemical class of pharmaceutical, designer, and experimental drugs. Contents …
47Elimination reaction — An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one or two step mechanism [JerryMarch] . Either the unsaturation of the molecule increases (as in most organic elimination… …
48Organophosphorus — compounds are degradable organic compounds containing carbon–phosphorus bonds (thus excluding from phosphate and phosphite esters, which lack such kind of bonding), used primarily in pest control as an alternative to chlorinated hydrocarbons that …
49Dichlorotris(triphenylphosphine)ruthenium(II) — IUPAC name Dic …
50N,N'-Dicyclohexylcarbodiimide — N,N Dicyclohexylcarbodiimide …
