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  2. Pyrrolidine - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine

    Pyrrolidine, also known as tetrahydropyrrole, is an organic compound with the molecular formula (CH 2) 4 NH. It is a cyclic secondary amine , also classified as a saturated heterocycle . It is a colourless liquid that is miscible with water and most organic solvents.

  3. Polybenzoxazine - Wikipedia

    en.wikipedia.org/wiki/Polybenzoxazine

    Benzoxazines are bicyclic heterocyclic compounds containing one oxygen and one nitrogen atom in a doubly unsaturated six-member ring, specifically a 1,3-oxazine ring, fused with a benzene ring. The systematic IUPAC name of the prototypical unsubstituted monomer is 3,4-dihydro-3-phenyl-2 H -1,3-benzoxazine.

  4. 3,4-Dihydropyran - Wikipedia

    en.wikipedia.org/wiki/3,4-dihydropyran

    3,4-Dihydropyran (DHP) is a heterocyclic compound with the formula C 5 H 8 O. The six-membered C 5 O ring has the unsaturation adjacent to oxygen. The isomeric 3,6-dihydropyran has a methylene separating the double bond and oxygen. DHP is used for protecting group for alcohols. It is a colorless liquid. [1]

  5. 1-Pyrroline-5-carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/1-Pyrroline-5-carboxylic_acid

    1-Pyrroline-5-carboxylic acid (systematic name 3,4-dihydro-2H-pyrrole-2-carboxylic acid [2]) is a cyclic imino acid. Its conjugate base and anion is 1-pyrroline-5-carboxylate (P5C). In solution, P5C is in spontaneous equilibrium with glutamate-5-semialdhyde (GSA).

  6. Dihydropyran - Wikipedia

    en.wikipedia.org/wiki/Dihydropyran

    In IUPAC names, "dihydro" refers to the two added hydrogen atoms needed to remove one double bond from the parent compound pyran. The numbers in front of the prefix indicate the position of the added hydrogen atoms (and not the position of the double bonds). [ 1 ]

  7. Nicotinonitrile - Wikipedia

    en.wikipedia.org/wiki/Nicotinonitrile

    Nicotinonitrile or 3-cyanopyridine is an organic compound with the formula NCC 5 H 4 N. The molecule consists of a pyridine ring with a nitrile group attached to the 3-position. A colorless solid, it is produced by ammoxidation of 3-methylpyridine: [2] H 3 CC 5 H 4 N + NH 3 + 1.5 O 2 → NCC 5 H 4 N + 3 H 2 O. Nicotinonitrile is a precursor to ...

  8. Phenylethylpyrrolidine - Wikipedia

    en.wikipedia.org/wiki/Phenylethylpyrrolidine

    1-(2-Phenylethyl)pyrrolidine (PEP) is a chemical compound. It is an analogue of 2-phenylethylamine where the amine has been replaced by a pyrrolidine ring . The β- keto derivative is phenacylpyrrolidine and the α- methyl and β-keto (i.e., cathinone ) derivative is α-pyrrolidinopropiophenone (α-PPP).

  9. N-(1-Naphthyl)ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N-(1-Naphthyl)ethylenediamine

    N-(1-Naphthyl)ethylenediamine dihydrochloride is widely used in the quantitative analysis of nitrate and nitrite in water samples by colorimetry. It readily undergoes a diazonium coupling reaction in the presence of nitrite to give a strongly colored azo compound .