90812-66-1

Basic information

• Product Name: 4-(CarboxyMethoxy)-benzoic acid Methyl ester
• Synonyms: 4-(CarboxyMethoxy)-benzoic acid Methyl ester;2-(4-(methoxycarbonyl)phenoxy)acetic acid;Benzoic Acid, 4-(Carboxymethoxy)-, 1-Methyl Ester
• CAS NO: 90812-66-1
• Molecular Formula: C₁₀H₁₀O₅
• Molecular Weight: 210.1834
• Mol File: 90812-66-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(CarboxyMethoxy)-benzoic acid Methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(CarboxyMethoxy)-benzoic acid Methyl ester(90812-66-1)
• EPA Substance Registry System: 4-(CarboxyMethoxy)-benzoic acid Methyl ester(90812-66-1)

Safety Data

• Hazardous Substances Data: 90812-66-1(Hazardous Substances Data)

Usage

General Description

4-(CarboxyMethoxy)-benzoic acid methyl ester is an organic compound with the chemical formula C10H10O5. It is a methyl ester derivative of 4-(carboxymethoxy)benzoic acid, and is often used as a precursor in the synthesis of pharmaceuticals and other organic compounds. 4-(CarboxyMethoxy)-benzoic acid Methyl ester is commonly used in organic chemistry research and is known for its ability to undergo various chemical reactions, making it a versatile building block in the development of new compounds. Its structure consists of a benzene ring attached to a carboxylic acid group and a methoxy group, with the methyl ester providing additional stability and reactivity to the molecule.

Upstream product

• 99-76-3 methyl 4-hydroxylbenzoate 
• 79-11-8 chloroacetic acid 
• 79-08-3 bromoacetic acid 
• 174666-21-8 4-t.-butoxycarbonylmethoxy-benzoic acid methyl ester 
• 19360-67-9 4-carboxymethoxy-benzoic acid 
• 35005-30-2 methyl 4-(2-methoxy-2-oxoethoxyl)benzoate 

Downstream Products

• 1256258-89-5 methyl 4-(2,2-dimethyl-4,15-dioxo-3,8,11-trioxa-5,14-diazahexadecan-16-yloxy)benzoate 
• 1096091-38-1 methyl 4-(2-(4-(naphthalen-2-ylsulfonyl)piperazin-1-yl)-2-oxoethoxy)benzoate 

Relevant articles and documents

Non-steroidal anti-inflammatory agents. Part 23: Synthesis and pharmacological activity of enaminones which inhibit both bovine cyclooxygenase and 5-lipoxygenase

The synthesis and stereochemical characteristics of pyrrolidino-, isoquinolino- and indolo-enaminones 2-11 are reported. The inhibition of cyclooxygenase was determined in a bovine thrombocyte intact cell assay and that of 5-lipoxygenase using intact bovine polymorphonuclear leucocytes. Except compound 2c′ which is a well-balanced dual inhibitor of both enzymes, all other enaminone derivatives are weak inhibitors of both cyclooxygenase and 5-lipoxygenase. Structure-activity relationships of the enaminones in relation to known anti-inflammatory drugs are discussed. Johann Ambrosius Barth 1998.

BENZODICYCLOALKANE DERIVATIVE, PREPARATION METHOD AND USE THEREOF

It is provided herein a benzobicycloalkane derivative, and a preparation method and use thereof. In particular, it is provided herein a compound of Formula (I), or a pharmaceutically acceptable salt, stereoisomer or solvate thereof, a preparation method, and a use thereof in preparation of drugs for treating pain.

Triazole derivatives

The present invention relates to triazole and imidazole derivatives of formula I and to their pharmaceutically acceptable acid addition salts. These compounds are NMDA receptor subtype blockers and are useful for the treatment of diseases related to the NMDA receptor.