3904-16-3

Usage

Uses

Used in Pharmaceutical Industry:
1-Amino-1-phenylacetone hydrochloride is used as a precursor for the synthesis of various pharmaceuticals and organic compounds. Its versatility in chemical reactions allows for the production of a wide range of medications and other organic products.
Used in Research and Development:
In the field of research and development, 1-Amino-1-phenylacetone hydrochloride serves as a valuable intermediate for the creation of new chemical entities. Its unique properties make it suitable for exploring novel chemical pathways and developing innovative applications in various industries.
Used in Controlled Substances Regulation:
As a controlled substance, 1-Amino-1-phenylacetone hydrochloride is used in the enforcement of laws and regulations related to the prevention of misuse and abuse of chemicals with potential for illicit applications. Its classification helps ensure that its production, distribution, and use are monitored and regulated to prevent unauthorized access and potential harm.

InChI:InChI=1/C9H11NO.ClH/c1-7(11)9(10)8-5-3-2-4-6-8;/h2-6,9H,10H2,1H3;1H

Upstream product

• 103-01-5 N-Phenylglycine 
• 103-79-7 1-phenyl-acetone 
• 25355-34-4 1-phenyl-propane-1,2-dione 1-oxime 

Downstream Products

• 54600-85-0 2,5-dimethyl-3,6-diphenylpyrazine 
• 107324-97-0 3-(4-Nitro-phenoxy)-N-(2-oxo-1-phenyl-propyl)-propionamide 
• 52500-61-5 2-hydroxy-1-phenylpropylamine 
• 1439370-60-1 7-(dimethylamino)-3-methyl-2-phenylchromeno[4,3-b]pyrrol-4(1H)-one 
• 1439370-58-7 4-((2-oxo-1-phenylpropyl)amino)-3-acetyl-7-dimethylaminocoumarin 
• 1439370-56-5 4-((2-oxo-1-phenylpropyl)amino)-3-benzoyl-7-dimethylaminocoumarin 
• 107325-11-1 sodium salt of 5-{4-[2-(5-methyl-4-phenyl-2-oxazolyl)ethoxy]benzyl}-2,4-thiazolidinedione 
• 107324-92-5 2-imino-5-{4-[2-(5-methyl-4-phenyl-2-oxazolyl)ethoxy]benzyl}-4-thiazolidinone 
• 107325-04-2 5-Methyl-2-[2-(4-nitro-phenoxy)-ethyl]-4-phenyl-oxazole 
• 141399-51-1 4-[2-(5-Methyl-4-phenyl-oxazol-2-yl)-ethoxy]-phenylamine 
• 88122-90-1 (+/-)-5c-methyl-2,4r-diphenyl-4,5-dihydro-oxazole 
• 88122-90-1 trans-5-methyl-2,4-diphenyl-Δ²-oxazoline 
• 131003-73-1 4-Methyl-N-(2-oxo-1-phenyl-propyl)-benzamide 
• 92962-80-6 N-(2-oxo-1-phenylpropyl)benzamide 

Relevant academic research and scientific papers

Synthesis of coumarin/pyrrole-fused heterocycles and their photochemical and redox-switching properties

Two coumarin/pyrrole-fused heterocycles were synthesized to investigate their photochemical and redox-switching properties. Photooxidation of the colorless diphenyl-substituted pyrrolocoumarin resulted in a distinct change to red and a sharp decrease in f

Anti-tumor compounds

The invention relates to quinazoline derivatives, or pharmaceutically-acceptable salts thereof, which possess anti-tumour activity; to processes for their manufacture; and to pharmaceutical compositions containing them. The invention provides a quinazoline of the formula: STR1 wherein R1 includes hydrogen, amino and alkyl or alkoxy each of up to 4 carbon atoms; R2 includes hydrogen, alkyl, hydroxyalkyl and halogenoalkyl each of up to 4 carbon atoms; R3 is hydrogen or alkyl or up to 3 carbon atoms; Ar is phenylene or heterocyclene; L is a group of the formula --CO.NH--, --NH.CO--, --CO.NR4 --, --NR4.CO--, --CH=CH-- or --CO.O--, wherein R4 is alkyl of up to 4 carbon atoms; and Y is a branched alkyl group bearing substituents Y2 and Y3 the definition of each independently including hydroxy, cyano, aryl and heteroaryl, and the definition of Y3 also optionally including sulpho, N-phenylsulphonylcarbamoyl and 5-tetrazolyl; or a pharmaceutically-acceptable salt thereof.

ISOQUINOLINE SYNTHESIS VIA 2-OXAZOLINES. PART VI. TRANSFORMATION OF 1-BENZAMIDO-1-PHENYL-2-ALKANOLS INTO 4-ALKYL-1-PHENYLISOQUINOLINES

Conditions necessary for the transformation of 1-benzamido-1-phenyl-2-alkanols (1) and 5-alkyl-2,4-diphenyl-2-oxazolines (2) into 4-alkyl-1-phenylisoquinolines (3) have been determined.The mechanism proposed for these reactions is supported by the results