77344-69-5

Usage

Uses

Used in Pharmaceutical Industry:
1-(2-chloro-5-methoxyphenyl)ethanone is used as a key intermediate for the synthesis of various drugs due to its chemical structure and properties.
Used in Perfume Industry:
1-(2-chloro-5-methoxyphenyl)ethanone is used as a key intermediate in the production of fragrances because of its slightly sweet, pungent odor.
Used in Organic Synthesis:
1-(2-chloro-5-methoxyphenyl)ethanone is used as a reagent in organic synthesis for the preparation of a wide range of other organic compounds.
Used in Building Blocks for Organic Compounds:
1-(2-chloro-5-methoxyphenyl)ethanone serves as a building block for the preparation of various organic compounds, making it a valuable component in the production of commercial products.
It is important to handle 1-(2-chloro-5-methoxyphenyl)ethanone with care as it can be harmful if not used properly.

Upstream product

• 103029-98-7 1-(2-chloro-5-methoxy-phenyl)-2-diazo-ethanone 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 6280-89-3 2-chloro-5-methoxybenzoic acid 
• 917-54-4 methyllithium 
• 100191-61-5 2-chloro-5-methoxybenzoic acid chloride 
• 506-82-1 dimethylcadmium 

Downstream Products

• 100712-48-9 [(Z)-1-(2-chloro-5-methoxy-phenyl)-ethylidene]-succinic acid 
• 100712-48-9 [(E)-1-(2-chloro-5-methoxy-phenyl)-ethylidene]-succinic acid 
• 58020-38-5 3-acetyl-4-chlorophenol 
• 76106-74-6 6-methoxy-3-phenyl-2,3-dihydro-1H-inden-1-one 
• 77172-79-3 [2-(2,4-Dichloro-phenoxy)-5-methoxy-phenyl]-acetic acid 
• 86308-69-2 [2-(2-Chloro-4-methyl-phenoxy)-5-methoxy-phenyl]-acetic acid 

Relevant academic research and scientific papers

Room temperature C(sp2)-H oxidative chlorination: Via photoredox catalysis

Photoredox catalysis has been developed to achieve oxidative C-H chlorination of aromatic compounds using NaCl as the chlorine source and Na2S2O8 as the oxidant. The reactions occur at room temperature and exhibit exclusive selectivity for C(sp2)-H bonds over C(sp3)-H bonds. The method has been used for the chlorination of a diverse set of substrates, including the expedited synthesis of key intermediates to bioactive compounds and a drug.

8-AZABICYCLO[3.2.1]OCTANE-8-CARBOXAMIDE DERIVATIVE

Disclosed is a compound represented by formula (1) or a pharmacologically acceptable salt thereof (In the formula, A represents a group that is represented by formula (A-1); R1a and R1b may be the same or different and each independently represents a C1-6 alkyl group which may be substituted by one to three halogen atoms; m and n each independently represents an integer of 0-5; X1 represents a hydroxyl group or an aminocarbonyl group; Z1 represents a single bond or the like; and R2 represents an optionally substituted C1-6 alkyl group, an optionally substituted C6-10 aryl group or the like.)