40359-30-6

Usage

Uses

Used in Pharmaceutical Research:
2-(2-Formyl-6-methoxyphenoxy)acetic acid is used as a building block in pharmaceutical research for the synthesis of various pharmaceuticals. Its unique structural features and functional groups make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 2-(2-Formyl-6-methoxyphenoxy)acetic acid is used as a starting material for the synthesis of herbicides and pesticides. Its structural characteristics and functional groups contribute to the development of effective and targeted agrochemicals for crop protection and weed management.
Used in Organic Synthesis:
2-(2-Formyl-6-methoxyphenoxy)acetic acid is employed as a versatile building block in organic synthesis. Its formyl and methoxy groups, along with the phenyl ring and acetic acid moiety, allow for a wide range of chemical reactions and transformations, making it a valuable component in the synthesis of various organic compounds for diverse applications.

InChI:InChI=1/C10H10O5/c1-14-8-4-2-3-7(5-11)10(8)15-6-9(12)13/h2-5H,6H2,1H3,(H,12,13)

Upstream product

• 70076-67-4 2-ethoxycarbonylmethoxy-3-methoxybenzaldehyde 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 79-11-8 chloroacetic acid 

Downstream Products

• 1415995-67-3 ethyl 2-[2-{bis(2-methyl-1H-indol-3-yl)methyl}-6-methoxyphenoxy]acetate 
• 1415995-25-3 ethyl 2-[2-{bis(1H-indol-3-yl)methyl}-6-methoxyphenoxy]acetate 
• 486995-89-5 2-{2-[bis(2-methyl-1H-indol-3-yl)methyl]-6-methoxyphenoxy}acetic acid 
• 486994-77-8 2-{2-bis[(1H-indol-3-yl)methyl]-6-methoxyphenoxy}acetic acid 
• 312291-67-1 2-(2-methoxy-6-(3,3,6,6-tetramethyl-1,8-dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl)phenoxy)acetic acid 

Relevant academic research and scientific papers

Organocatalytic Synthesis of Fused Bicyclic 2,3-Dihydro-1,3,4-oxadiazoles through an Intramolecular Cascade Cyclization

Hydrazone-carboxylic acids undergo intramolecular cyclization in the presence of pivaloyl chloride, iPr2NEt, and catalytic DABCO to form a range of substituted fused tricyclic 2,3-dihydro-1,3,4-oxadiazoles in high yields.

An efficient one pot syntheses of aryl-3,3′-bis(indolyl)methanes and studies on their spectral characteristics, DPPH radical scavenging-, antimicrobial-, cytotoxicity-, and antituberculosis activity

An efficient one-pot syntheses of aryl-3,3′-bis(indolyl)methanes (BIMs) from indole/2-methylindole and formylphenoxyaliphatic acid(s) is described. Esterification of carboxylic acid and aromatic electrophilic substitution reactions are achieved simultaneous in the presence of potash alum as a catalyst. This catalyst could be recovered and reused without substantial loss in its catalytic activity and the methodology could be applied on a range of closely related substrates. The solvation characteristics in ground and excited states of the compounds by monitoring the absorbance and fluorescence band maxima have been studied. The fluorescence studies in protic and aprotic solvents were rationalized on the basis of solute-solvent interaction and substituents effect on these photophysical processes analyzed. The compounds prepared showed efficient antimicrobial effect against human pathogens, cytotoxicity against A431 cell line, and DPPH radical scavenging effect. Single crystal XRD studies have been carried out for a few compounds synthesized in this work.

Oxime derivatives of cephalosporanic structure

The invention relates to oxime derivatives of cephalosporanic structure, possessing antibacterial activity.

Oxime derivatives of cephalosporanic structure and compounds for their preparation

The invention relates to oxime derivatives of cephalosporanic structure, possessing antibacterial activity of the following formula: where X, Y, Z, A, n, R and R1 are as specified in the description.