64605-34-1

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(2-amino-5-methoxyphenyl)-2-chlorois used as a potential drug candidate for its structural features that may contribute to the development of new therapeutic agents. Its chemical properties, such as the presence of a chloro-substituted aromatic ring, amine, and methoxy group, could be exploited in the design of novel drugs with specific pharmacological activities.
Used in Medicinal Chemistry Research:
Ethanone, 1-(2-amino-5-methoxyphenyl)-2-chlorois used as a research compound in medicinal chemistry to explore its potential biological activities and interactions with biological targets. Further studies and research are needed to fully understand its potential uses and to optimize its properties for specific therapeutic applications.

Upstream product

• 104-94-9 4-methoxy-aniline 
• 107-14-2 chloroacetonitrile 

Downstream Products

• 400017-84-7 2-[2-(2-amino-5-methoxy-phenyl)-2-oxo-ethyl]-2-butyrylamino-malonic acid diethyl ester 
• 400017-83-6 2-acetylamino-2-[2-(2-amino-5-methoxy-phenyl)-2-oxo-ethyl]-malonic acid diethyl ester 
• 1335060-74-6 (Z)-allyl 3-[1-(3,4-dimethoxybenzyloxy)ethyl]-2-(hex-3-ene-1,5-diynyl)-4-hydroxymethyl-6-methoxyquinoline-1(2H)-carboxylate 
• 1335136-65-6 (Z)-allyl 1a-[1-(3,4-dimethoxybenzyloxy)ethyl]-2-(hex-3-ene-1,5-diynyl)-7b-(hydroxymethyl)-6-methoxy-1a,2-dihydrooxireno[2,3-c]quinoline-3(7bH)-carboxylate 
• 1335136-66-7 (Z)-allyl 1a-[1-(3,4-dimethoxybenzyloxy)ethyl]-7b-formyl-2-(hex-3-ene-1,5-diynyl)-6-methoxy-1a,2-dihydrooxireno[2,3-c]quinoline-3(7bH)-carboxylate 
• 1335060-60-0 4-[2-(2-acetyloxyacetyl)-4-methoxyphenylamino]butan-2-one 
• 1335060-57-5 4-tert-butyldimethylsilyloxymethyl-3-[1-(3,4-dimethoxybenzyloxy)ethyl]-6-methoxyquinoline 
• 1335060-80-4 1-(2-amino-5-methoxyphenyl)-2-acetyloxyethanone 
• 1335060-51-9 4-[2-(2-chloroacetyl)-4-methoxyphenylamino]butan-2-one 
• 340169-29-1 5-methoxy-3-(phenylsulfanyl)-1H-indole 

Relevant academic research and scientific papers

Setbacks and hopes: En route to the synthesis of uncialamycin

We herein report a new approach toward the synthesis of uncialamycin, an enediyne natural product isolated from the Streptomyces uncialis, bacteria present on the surface of the lichen Cladonia uncialis. A model for the preparation of uncialamycin has bee

Synergistic Cooperative Effect of Sodium borohydride-Iodine Towards Cascade C?N and C?S/Se Bond Formation: One-pot Regioselective Synthesis of 3-Sulfenyl/selenyl Indoles and Mechanistic Insight

In this work, a new strategy to synthesize 3-sulfenyl/selenyl indole is reported wherein LC?MS reveals a novel insight into synergistic cooperative effect of NaBH4-I2 which allows cascade C?N and C?S/C?Se bond formations via reduction-nucleophilic cyclization-chalcogenylation, three steps in one-pot, towards regioselective synthesis of diverse 3-chalcogenyl indoles including 5-bromo-3-[(3,4,5-trimethoxyphenyl)thio]-1H-indole, a known lead anticancer compound, directly from 2-amino-phenacylchlorides and thiophenols or disulfides/diselenides in aqueous dioxane under transition-metal-free condition. (Figure presented.).