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1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2. It is used as a solvent , as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers , and pharmaceutical products, [ 1 ] and as a flavoring agent .
Aminopentane may refer to: 1-Aminopentane; 2-Aminopentane; 3-Aminopentane This page was last edited on 4 August 2019, at 16:05 (UTC). Text is available under the ...
Cyanoethylation is a process for the attachment of CH 2 CH 2 CN group to another organic substrate. The method is used in the synthesis of organic compounds. [1] Cyanoethylation entails addition of protic nucleophiles to acrylonitrile. Typical protic nucleophiles are alcohols, thiols, and amines. Two new bonds form: C-H and C-X (X = carbon ...
A 1,2-rearrangement or 1,2-migration or 1,2-shift or Whitmore 1,2-shift [1] is an organic reaction where a substituent moves from one atom to another atom in a chemical compound. In a 1,2 shift the movement involves two adjacent atoms but moves over larger distances are possible. In the example below the substituent R moves from carbon atom C 2 ...
1-Phenyl-2-propylaminopentane (PPAP; developmental code name MK-306) is an experimental drug related to selegiline which acts as a catecholaminergic activity enhancer (CAE). [1] [2] [3] [4]
November 23, 2024 at 2:23 PM Surveillance photo of the suspect and the building near the crime scene. An Italian tourist was slashed in the hand by a stranger in an unprovoked attack in Midtown ...
Nearly 18 years after accusing three Duke University students of raping her, an account she shared in explicit and graphic detail, — Magnum has admitted she lied about the whole thing.
A Norrish type II reaction is the photochemical intramolecular abstraction of a γ-hydrogen (a hydrogen atom three carbon positions removed from the carbonyl group) by the excited carbonyl compound to produce a 1,4-biradical as a primary photoproduct. [9] Norrish first reported the reaction in 1937. [10] Norrish type II reaction