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Piperidine is an organic compound with the molecular formula (CH 2) 5 NH. This heterocyclic amine consists of a six-membered ring containing five methylene bridges (–CH 2 –) and one amine bridge (–NH–). It is a colorless liquid with an odor described as objectionable, typical of amines. [6]
The platinichloride B 4 ·H 2 PtCl 6 forms orange-red needles ("B" denotes one mole of the alkaloid base in this and the following formula). Iodine in potassium iodide added to an alcoholic solution of the base in the presence of a little hydrochloric acid gives a characteristic periodide, B 2 ·HI·I 2 , crystallizing in steel-blue needles ...
The molecular formula C 5 H 11 N (molar mass: 85.15 g/mol, exact mass: 85.0891 u) may refer to: Piperidine (hexahydropyridine) Cyclopentylamine (cyclopentanamine) 1-Methylpyrrolidine; 2-Methylpyrrolidine
Heterocyclic organic compounds can be usefully classified based on their electronic structure. The saturated organic heterocycles behave like the acyclic derivatives. Thus, piperidine and tetrahydrofuran are conventional amines and ethers, with modified steric profiles. Therefore, the study of organic heterocyclic chemistry focuses on organic ...
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
The chemical is part of the piperidine family, [1] along with many pharmaceuticals and alkaloids such as piperine, which gives black pepper its spicy taste. Trade names include Bayrepel and Saltidin among others. The compound was developed by the German chemical company Bayer in the 1980s [6] and was given the name Bayrepel.
N-Formylpiperidine is an organic compound with the formula C 6 H 11 NO. It is the amide of formic acid and piperidine. It can be used as a polar aprotic solvent, with better hydrocarbon solubility than other amide solvents such as dimethylformamide (DMF). [1] It has also been used to transfer the formyl group to a Grignard reagent: [2]
2,6-Dimethylpiperidines are chemical compounds with the formula C 5 H 8 (CH 3) 2 NH. Three stereoisomers exist: the achiral (R,S)-isomer and the chiral (R,R)/(S,S) enantiomeric pair. . Dimethylpiperidines are derivatives of the heterocycle piperidine, wherein two hydrogen atoms are replaced by methyl grou