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It reacts with amines to afford N-substituted benzamides after hydrolysis. [3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis. [4] Benzonitrile forms coordination complexes with transition metals that are both soluble in organic solvents and conveniently labile. One example is PdCl 2 ...
1,2-Dimethoxybenzene 1,3-Dimethoxybenzene 1,4-Dimethoxybenzene Structural Formula: CAS Registry Number: 91-16-7 151-10-0 150-78-7 All isomers share the molecular ...
Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH 3) 2 C 4 H 4. It is colorless liquid which served an important role in the early history of synthetic rubber. It is now a specialty reagent.
1,3-Dimethoxybenzene is an organic compound with the formula C 6 H 4 (OCH 3) 2. It is one of three isomers of dimethoxybenzene. Uses. 1,3-Dimethoxybenzene has been ...
2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene , it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene .
General structure of 25-NB derivatives, where R is usually 2,5-dimethoxy-4-(alkyl or halogen), R 1 is usually H but rarely methyl, and Cyc is usually 2-substituted phenyl but can be other heterocycles.
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inhaled carbon monoxide induces unconsciousness in 2–3 breaths and death in < 3 min (12 800 ppm) [15] 10 −3: mM 0.32–32 mM: normal range of hydronium ions in stomach acid (pH 1.5–3.5) [16] 5.5 mM: upper bound for healthy blood glucose when fasting [17] 7.8 mM: upper bound for healthy blood glucose 2 hours after eating [17] 10 −2: cM 20 mM