54023-06-2

Basic information

• Product Name: 5-(3-AMINOPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER
• Synonyms: SALOR-INT L300594-1EA;CBI-BB ZERO/008739;METHYL 5-(3-AMINOPHENYL)FURAN-2-CARBOXYLATE;5-(3-AMINOPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER;METHYL 5-(3-AMINOPHENYL)FURAN-2-CARBOXY&
• CAS NO: 54023-06-2
• Molecular Formula: C₁₂H₁₁NO₃
• Molecular Weight: 217.22
• Mol File: 54023-06-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 102-106 °C(lit.)
• Boiling Point: 411.2 °C at 760 mmHg
• Flash Point: 202.5 °C
• Appearance: /
• Density: 1.222 g/cm³
• CAS DataBase Reference: 5-(3-AMINOPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-AMINOPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER(54023-06-2)
• EPA Substance Registry System: 5-(3-AMINOPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER(54023-06-2)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 54023-06-2(Hazardous Substances Data)

Usage

General Description

5-(3-aminophenyl)furan-2-carboxylic acid methyl ester is a chemical compound with the molecular formula C13H11NO3. It is a methyl ester derivative of 5-(3-aminophenyl)furan-2-carboxylic acid, which is a heterocyclic compound containing both furan and carboxylic acid functional groups. This chemical may be used in the pharmaceutical industry as a building block for the synthesis of potential drugs or as a research tool in the study of furan-containing compounds. It has potential applications in the development of new drugs for various diseases and conditions due to its unique chemical structure and properties. However, further research and testing are needed to fully understand its potential uses and effects.

Upstream product

• 41019-37-8 5-(3-nitrophenyl)-furan-2-carboxylic acid methyl ester 
• 13130-13-7 5-(3-nitro-phenyl)-furan-2-carboxylic acid 
• 2527-99-3 methyl 5-bromo-2-furoate 
• 13331-27-6 m-nitrobenzene boronic acid 
• 585-70-6 5-bromo-furan-2-carboxylic acid 
• 30418-59-8 3-Aminophenylboronic acid 

Downstream Products

• 942232-15-7 C₃₄H₃₈N₄O₆ 
• 528885-24-7 5-(3-(2-(5-cyclohexyl-1-(3,3-dimethyl-2-oxo-butyl)-2-oxo-1,2-dihydro-3H-1,3,4-benzotriazepin-3-yl)-acetylamino)-phenyl)-furan-2-carboxylic acid 

Relevant articles and documents

Design, synthesis, and electrophysiological evaluation of NS6740 derivatives: Exploration of the structure-activity relationship for alpha7 nicotinic acetylcholine receptor silent activation

The α7 nicotinic acetylcholine receptor (nAChR) silent agonists, able to induce receptor desensitization and promote the α7 metabotropic function, are emerging as new promising therapeutic anti-inflammatory agents. Herein, we report the structure–activity

Optimization of 1,3,4-benzotriazepine-based CCK2 antagonists to obtain potent, orally active inhibitors of gastrin-mediated gastric acid secretion

Starting from a novel, achiral 1,3,4-benzotriazepine-based CCK2 receptor antagonist, a process of optimization has afforded further compounds of this type that maintain the nanomolar affinity for recombinant, human CCK2 receptors and high selectivity over

AMINO ACIDS

Compounds of formula (I): Z’ -CO-A-B-NH-Z (I) wherein: Z is H or an amino protecting group; Z’ is OH, a protected or activated hydroxyl group or C1; A is an optionally substituted C5-6 arylene group; and B is an optionally substituted C5-6 arylene group.