63874-38-4

Basic information

• Product Name: Benzoic acid, 3-(aminocarbonyl)-4-hydroxy-, methyl ester
• Synonyms: 4-hydroxy-isophthalamic acid methyl ester;4-Hydroxy-isophthalamidsaeure-methylester;5-carbomethoxysalicylamide;methyl 3-carbamoyl-4-hydroxybenzoate
• CAS NO: 63874-38-4
• Molecular Formula: C9H9NO4
• Molecular Weight: 195.175
• Mol File: 63874-38-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 230 °C
• Boiling Point: 352.4±32.0 °C(Predicted)
• Density: 1.351±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzoic acid, 3-(aminocarbonyl)-4-hydroxy-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-(aminocarbonyl)-4-hydroxy-, methyl ester(63874-38-4)
• EPA Substance Registry System: Benzoic acid, 3-(aminocarbonyl)-4-hydroxy-, methyl ester(63874-38-4)

Safety Data

• Hazardous Substances Data: 63874-38-4(Hazardous Substances Data)

Usage

General Description

Benzoic acid, 3-(aminocarbonyl)-4-hydroxy-, methyl ester, also known as methyl 3-(aminocarbonyl)-4-hydroxybenzoate, is a chemical compound with the formula C9H9NO4. It is commonly used as a flavoring agent and preservative in various food and beverage products. It is also utilized in cosmetic and pharmaceutical products as a fragrance ingredient. The compound has antimicrobial properties, making it effective in preserving products and preventing the growth of bacteria and fungi. It is important to use this chemical compound in accordance with safety guidelines to avoid any potential health risks.

Upstream product

• 79128-78-2 2-hydroxy-5-(methoxycarbonyl)benzoic acid 
• 636-46-4 4-hydroxyisophthalic acid 
• 94633-02-0 methyl 4-benzyloxy-3-carbamoylbenzoate 
• 67-56-1 methanol 
• 76142-87-5 5-carboxysalicylamide 
• 5985-24-0 dimethyl 4-hydroxyisophthalate 

Downstream Products

• 24798-47-8 2-(2-hydroxy-5-methoxycarbonylphenyl)-4H-1,3-benzoxazin-4-one 
• 1431546-52-9 C₂₅H₃₁N₃O₅ 
• 76142-87-5 5-carboxysalicylamide 

Relevant articles and documents

MONOMERS CAPABLE OF DIMERIZING IN AN AQUEOUS SOLUTION, AND METHODS OF USING SAME

Described herein are monomers capable of forming a biologically useful multimer when in contact with one, two, three or more other monomers in an aqueous media. In one aspect, such monomers may be capable of binding to another monomer in an aqueous media (e.g. in vivo) to form a multimer, (e.g. a dimer). Contemplated monomers may include a ligand moiety, a linker element, and a connector element that joins the ligand moiety and the linker element. In an aqueous media, such contemplated monomers may join together via each linker element and may thus be capable of modulating one or more biomolecules substantially simultaneously, e.g., modulate two or more binding domains on a protein or on different proteins.

Modulators of Acetyl-Coenzyme A Carboxylase and Methods of Use Thereof

The present invention provides compounds of formula I: along with methods of use of these compounds as pharmaceuticals, particularly in the treatment of obesity, metabolic syndrome, atherosclerosis, cardiovascular disease, insulin resistance, diseases ass