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Jul 27, 2023 · N-Alkyl amines are prevalent compounds in organic synthesis and medicinal chemistry; however, their synthesis can be impeded by the availability of key reaction components and low selectivity. Now ...
Apr 29, 2024 · Chemical Synthesis Database. ChemSynthesis is a freely accessible database of chemicals. This website contains substances with their synthesis references and physical properties such as melting point, boiling point and density. There are currently more than 40,000 compounds and more than 45,000 synthesis references in the database.
Sep 24, 2006 · Synthesis and Properties of Phenyl Cyclohexyl Ferroelectric Liquid Crystals Sun Yongmao Department of Chemistry, Tsinghua University, Beijing, 100084, People's Republic of China Yu Hongping Department of Chemistry, Tsinghua University, Beijing, 100084, People's Republic of China
May 1, 1990 · Synthesis of PCDTBT-Based Fluorinated Polymers for High Open-Circuit Voltage in Organic Photovoltaics: Towards an Understanding of Relationships between Polymer Energy Levels Engineering and Ideal Morphology Control; Colloidal Synthesis of Strongly Fluorescent CsPbBr3 Nanowires with Width Tunable down to the Quantum Confinement Regime
Phenyl-2-nitropropene (Methylamine Catalysis) Written by GC_MS. Phenyl-2-Nitropropene à la Barium: 1 mol benzaldehyde, 1.2 mol nitroethane and 15 mL diluted aqueous methylamine in 150 mL alcohol. Stirred and slightly heated for ca 4 hours. The reaction mixture is brought over into a beaker and cooled in the fridge (4°C).
Feb 6, 2010 · IUPAC Standard InChI: InChI=1S/C12H23N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h11-13H,1-10H2 Copy IUPAC Standard InChIKey: XBPCUCUWBYBCDP-UHFFFAOYSA-N Copy CAS Registry ...
Phenylamine reacts with acids like hydrochloric acid in exactly the same way as any other amine. Despite the fact that the phenylamine is only a very weak base, with a strong acid like hydrochloric acid the reaction is completely straightforward. Phenylamine is only very slightly soluble in water, but dissolves freely in dilute hydrochloric acid.
