40754-13-0

Basic information

• Product Name: 2'-AMINOACETOPHENONE PHENYLHYDRAZONE
• Synonyms: 2'-AMINOACETOPHENONE PHENYLHYDRAZONE;2'-AMINOACETOPHENONE PHENYLHYDRAZONE, 97 %;(E)-2-(1-(2-PHENYLHYDRAZONO)ETHYL)ANILINE
• CAS NO: 40754-13-0
• Molecular Formula: C₁₄H₁₅N₃
• Molecular Weight: 225.29
• Product Categories: Hydrazones;Nitrogen Compounds;Organic Building Blocks
• Mol File: 40754-13-0.mol
• Article Data: 9

Chemical Properties

• Melting Point: 104-108 °C(lit.)
• Appearance: /
• CAS DataBase Reference: 2'-AMINOACETOPHENONE PHENYLHYDRAZONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-AMINOACETOPHENONE PHENYLHYDRAZONE(40754-13-0)
• EPA Substance Registry System: 2'-AMINOACETOPHENONE PHENYLHYDRAZONE(40754-13-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 40754-13-0(Hazardous Substances Data)

Usage

General Description

2'-Aminoacetophenone phenylhydrazone is a chemical compound that belongs to the class of hydrazones. It is an organic compound with the molecular formula C14H14N4O and a molar mass of 250.29 g/mol. 2'-AMINOACETOPHENONE PHENYLHYDRAZONE is often used as a reagent in chemical reactions and as a building block in the synthesis of other organic compounds. It is known for its ability to form coordination complexes with various metal ions, and it has been studied for its potential biological and pharmacological activities. Overall, 2'-aminoacetophenone phenylhydrazone is a versatile chemical with various applications in both research and industrial settings.

Upstream product

• 551-93-9 2-aminoacetophenone 
• 100-63-0 phenylhydrazine 

Downstream Products

• 1401404-43-0 6-(4-bromophenyl)-11H-indolo[3,2-c]quinoline 
• 1401404-44-1 6-(4-chlorophenyl)-11H-indolo[3,2-c]quinoline 
• 1239778-88-1 6-(4-chlorophenyl)indolo[1,2-c]quinazoline 
• 1448807-86-0 6-(4-nitrophenyl)-indolo[1,2-c]quinazoline 
• 1385821-07-7 6-(4-methoxyphenyl)-indolo[1,2-c]quinazoline 
• 1239778-99-4 6-(p-tolyl)indolo[1,2-c]quinazoline 
• 1401404-46-3 6-(4-methylphenyl)-11H-indolo[3,2-c]quinoline 
• 4295-28-7 6-methyl-11H-indolo[3,2-c]-quinoline 
• 239-09-8 11H-indolo[3,2-c]quinoline 

Relevant articles and documents

Selective C?H or N?H Imidoylative Annulation of 2-(2-Isocyanophenyl)-1H-indoles Leading to Diverse Indole-fused Scaffolds

2-(2-Isocyanophenyl)-1H-indoles, a class of functionalized isocyanides containing both aromatic C?H and indolo N?H functionalities, are first applied in selective imidoylative annulation reactions. Scaffolds of 6-aryl 11H-indolo[3,2-c]quinoline and 6-aryl

A nitroalkane-based approach to one-pot three-component synthesis of isocryptolepine and its analogs with potent anti-cancer activities

A second generation polyphosphoric acid-mediated one-pot three-component synthesis of indoloquinoline scaffold is developed. This improved version of the process involves electrophilically activated nitroalkanes for the installation of strategic C-C and C-N bonds and ring C assembly. This modification allows the elimination of unnecessary solvent change operations and all steps are carried out in a true, uninterrupted one-pot manner. A further improvement involves the possibility to install an ortho-amino group in situ. A synthetic application of this method is showcased by the concise synthesis of an isocryptolepine alkaloid and its synthetic analogs with potent anticancer activities.

A new compound and an organic electronic device using the same

The present invention provides a new compound and an organic electronic device using the same. The compound according to the present invention may serve as hole injection, hole transporting, electron injection and transporting, and light emitting materials and the like in an organic electronic device comprising an organic light emitting device, and the organic electronic device according to the present invention shows excellent properties in terms of efficiency, driving voltage and service life.