84923-70-6

Usage

Uses

Used in Pharmaceutical Industry:
5-Formyl-2-methoxybenzoic Acid is used as an intermediate for the synthesis of various pharmaceuticals due to its versatile reactivity and stability. It plays a crucial role in the development of new drugs and the improvement of existing ones.
Used in Dye Industry:
5-Formyl-2-methoxybenzoic Acid is used as a precursor in the production of dyes. Its unique chemical structure allows for the creation of a wide range of colors, making it a valuable component in the dye industry.
Used in Flavoring Agents:
5-Formyl-2-methoxybenzoic Acid is used as a flavoring agent in the food industry. Its ability to react with other compounds to form esters contributes to the enhancement of flavors in various food products.
Used in Fine Chemicals Production:
5-Formyl-2-methoxybenzoic Acid is used as an intermediate in the production of fine chemicals. Its stability and reactivity make it an essential component in the synthesis of high-quality specialty chemicals.

InChI:InChI=1/C9H8O4/c1-13-8-3-2-6(5-10)4-7(8)9(11)12/h2-5H,1H3,(H,11,12)

Upstream product

• 78515-16-9 methyl 5-formyl-2-methoxybenzoate 
• 34841-06-0 3-bromo-4-methoxybenzylaldehyde 
• 201230-82-2 carbon monoxide 
• 616-76-2 2-hydroxy-5-formylbenzoic acid 
• 69-72-7 salicylic acid 
• 41489-76-3 methyl-5-formyl-2-hydroxybenzoate 

Downstream Products

• 311770-86-2 benzyl 5-formyl-2-methoxybenzoate 
• 311770-60-2 ethyl 2-ethoxy-3-(4-methoxy-3-({[4-(trifluoromethyl)benzyl]amino}carbonyl)phenyl)propanoate 
• 311771-06-9 2-[4-methoxy-3-(4-trifluoromethyl-benzylcarbamoyl)-benzyl]-pentanoic acid ethyl ester 
• 311771-14-9 2-[4-methoxy-3-(4-trifluoromethyl-benzylcarbamoyl)-benzyl]-hexanoic acid ethyl ester 
• 311770-61-3 3-[4-methoxy-3-(4-trifluoromethyl-benzylcarbamoyl)-phenyl]-2-phenoxy-propionic acid ethyl ester 
• 311770-92-0 methyl 3-(3-carboxy-4-methoxyphenyl)-2,2-dimethylpropanoate 
• 1025973-67-4 5-(2-ethyl-2-methoxycarbonyl-butyl)-2-methoxy-benzoic acid 
• 433283-41-1 2-(3-benzylcarbamoyl-4-methoxy-benzyl)-butyric acid ethyl ester 

Relevant academic research and scientific papers

OLEFIN SUBSTITUTED OXINDOLES HAVING AMPK ACTIVITY

The present invention relates to compounds of formula (I), which have valuable pharmacological properties, in particular are activators of AMPK and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

Synthesis of aromatic carboxylic acids by carbonylation of aryl halides in the presence of epoxide-modified cobalt carbonyls as catalysts

A new procedure was developed for synthesis of aromatic and heteroaromatic acids and their derivatives (esters, salts) by carbonylation of the corresponding aryl halides. The acids are selectively formed in a high yield under very mild conditions. Highly active catalytic systems, base-containing alcoholic solutions of cobalt carbonyl modified with epoxides, were used to activate aryl halides. 2005 Pleiades Publishing, Inc.

Thiazolidine derivatives and its use as antifungal agent

Compounds of formula (I) or salts thereof are provided wherein X is O or S, A and B are OR2 or Y—NR3R4 wherein when A is OR2. B is Y—NR3R4 and vice versa, or when one of A or B is OR2. then the other can be CO2R7. Y is CH2 or C=Q. Q is (CH2)m—CH(R1)—(CH2)n, R is OR6 or NHR7. and with the other definitions as set out in claim 1, a process for its preparation and its use in the prophylaxis or treatment of fungal infections. 1

Design, synthesis and evaluation of substituted phenylpropanoic acid derivatives as peroxisome proliferator-activated receptor (PPAR) activators: Novel human PPARα-selective activators

A series of substituted phenylpropanoic acid derivatives was prepared as part of a search for subtype-selective human peroxisome proliferator-activated receptor (PPAR) activators. Structure-activity relationship studies indicated that the substituent at the α-position of the carboxyl group plays a key role in determining the potency and the selectivity for PPAR transactivation.