40757-20-8

Usage

Uses

Used in Pharmaceutical Industry:
METHYL 4-METHOXY-3-NITROBENZOATE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential medicinal applications, particularly due to its anti-inflammatory and analgesic properties.
Used in Fragrance Industry:
METHYL 4-METHOXY-3-NITROBENZOATE is used as a fragrance ingredient, capitalizing on its unique scent profile to enhance the olfactory characteristics of various products.
Used in Cosmetic Industry:
In the cosmetic industry, METHYL 4-METHOXY-3-NITROBENZOATE is utilized as a flavoring agent, contributing to the sensory experience of cosmetic products.
Used in Food Industry:
METHYL 4-METHOXY-3-NITROBENZOATE is employed as a flavoring agent in the food industry, where it imparts specific taste and aroma profiles to enhance the consumer's culinary experience.

InChI:InChI=1/C9H9NO5/c1-14-8-4-3-6(9(11)15-2)5-7(8)10(12)13/h3-5H,1-2H3

Upstream product

• 121-98-2 methyl 4-methoxybenzoate 
• 89-41-8 4-methoxy-3-nitrobenzoic acid 
• 616-82-0 3-nitro-4-hydroxybenzoic acid 
• 14719-83-6 methyl 3-nitro-4-chlorobenzoate 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 

Downstream Products

• 24812-90-6 methyl 3-amino-4-methoxybenzoate 
• 127140-69-6 de(N-methyl)-N-formyl clarithromycin 
• 2840-26-8 3-amino-4-methoxybenzoic acid 
• 37908-98-8 methyl 3-chloro-p-anisate 
• 37908-96-6 3-chloro-4-methoxy benzoic acid 

Relevant academic research and scientific papers

FUSED BICYCLIC COMPOUNDS AND USES THEREOF IN MEDICINE

Fused bicyclic compounds and uses thereof in medicine. In particular, provided are fused bicyclic compounds used as ASK1 active regulator and and use of the compounds in the manufacture of a drug for treating a disease regulated by ASK1. Further provided are a pharmaceutical composition and a method of treating a disease regulated by ASK1 comprising administering the compounds or pharmaceutical composition thereof.

Synthetic triple helix-forming compound precursors

The present invention discloses novel monomeric compositions which are substituted quinoline- or quinazoline-based structures capable of hydrogen bonding specifically with interstrand purine-pyrimidine base pairs in a double-stranded Watson-Crick DNA mole

Process for the preparation of aromatic methyl methoxycarboxylates

The invention relates to a preparation process for aromatic methyl methoxycarboxylates by reaction of aromatic hydroxycarboxylic acids in the form of a mixture with the methoxycarboxylic acids with dimethyl sulphate in water.

Cerium(IV)-induced nitration of cinnamic acids. Novel remote electrophilic substitution

The treatment of (E)-3,4-dimethoxycinnamic acid with ceric amonium nitrate in trifluoroacetic acid afforded (E)1,2-dimethoxy-4-nitro-5-(2-nitroethenyl)benzene in 79percent yield.The unusual ipso substitution of the carboxylic acid moiety by a nitro functional center illustrated a new reaction manifold of cerium(IV).Six cinnamic acids were examined to ascertain the generality of the transformation.The bidentate nitrato structure of the metal salt is believed to account for the nitrating ability of this system.