4425-73-4

Basic information

• Product Name: 9-FLUORENYLIDENEACETIC ACID
• Synonyms: BIPHENYLENEACRYLIC ACID;9-FLUORENYLIDENEACETIC ACID;9H-fluoren-9-ylideneacetic acid;dibenzofulvene-1-carboxylic acid;Biphenylenecrylic acid;9H-Fluorene-9-ylideneacetic acid;2-(9H-Fluoren-9-ylidene)acetic acid
• CAS NO: 4425-73-4
• Molecular Formula: C₁₅H₁₀O₂
• Molecular Weight: 222.24
• EINECS: 224-604-0
• Mol File: 4425-73-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 231-233°C
• Boiling Point: 385.7°Cat760mmHg
• Flash Point: 284.1°C
• Appearance: /
• Density: 1.387g/cm³
• Vapor Pressure: 1.22E-06mmHg at 25°C
• CAS DataBase Reference: 9-FLUORENYLIDENEACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 9-FLUORENYLIDENEACETIC ACID(4425-73-4)
• EPA Substance Registry System: 9-FLUORENYLIDENEACETIC ACID(4425-73-4)

Safety Data

• Hazardous Substances Data: 4425-73-4(Hazardous Substances Data)

Usage

General Description

9-FLUORENYLIDENEACETIC ACID is a chemical compound with the molecular formula C15H12O2. It is often used in organic synthesis, and it is known for its ability to facilitate the formation of peptide bonds in peptide synthesis. 9-FLUORENYLIDENEACETIC ACID has also been studied for its potential use as a plant growth regulator, with research indicating that it may have the ability to promote the growth and development of various plants. Additionally, 9-FLUORENYLIDENEACETIC ACID has been investigated for its potential anti-inflammatory and anti-cancer properties, making it a subject of interest in medicinal chemistry research. Overall, 9-FLUORENYLIDENEACETIC ACID is a versatile compound with various potential applications in both chemical synthesis and biological studies.

InChI:InChI=1/C15H10O2/c16-15(17)9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-9H,(H,16,17)/p-1

Upstream product

• 18083-73-3 <9-Brom-fluorenyl-(9)>-bromessigsaeure-aethylester 
• 13461-74-0 9-ethynylfluoren-9-ol 
• 486-25-9 9-fluorenone 
• 872280-79-0 ethyl 2-(9H-fluoren-9-yl)-2-hydroxyacetate 
• 105-36-2 ethyl bromoacetate 
• 18083-76-6 Fluorenyliden-bromessigsaeure 
• 18083-74-4 Fluorenyliden-bromessigsaeure-ethylester 
• 27973-36-0 dibenzofulvenecarboxylic acid ethyl ester 
• 141-52-6 sodium ethanolate 
• 4425-71-2 2-(9H-fluoren-9-ylidene)acetaldehyde 

Downstream Products

• 19656-55-4 2-Phenyl-3.3-(o-biphenylen)-bernsteinsaeure 
• 1569819-69-7 (R)-N-(2-(9H-fluoren-9-ylidene)ethyl)-1-(4-fluorophenyl)ethanamine 
• 1569820-57-0 (R)-N-(2-(9H-fluoren-9-ylidene)ethyl)-1-(4-fluorophenyl)ethanamine 
• 65779-24-0 3-{4-[2-(2-Fluoren-9-ylidene-acetylamino)-ethyl]-phenyl}-propionic acid 
• 1195760-41-8 N-(2-aminophenyl)-6-(6-(2-(9H-fluoren-9-ylidene)acetamido)-hexylamino)nicotinamide 
• 1195760-27-0 N-(2-amino-4-trifluoromethyl-phenyl)-6-(2-(2-(9H-fluoren-9-ylidene)acetamido)ethylamino)-nicotinamide 
• 1195760-25-8 N-(2-amino-4-methoxyphenyl)-6-(2-(2-(9H-fluoren-9-ylidene)-acetamido)ethylamino)-nicotinamide 
• 1195760-23-6 N-(2-amino-4-methylphenyl)-6-(2-(2-(9H-fluoren-9-ylidene)-acetamido)ethylamino)-nicotinamide 
• 1195760-21-4 N-(2-amino-4-chlorophenyl)-6-(2-(2-(9H-fluoren-9-ylidene)-acetamido)ethylamino)-nicotinamide 
• 1195760-19-0 N-(2-amino-4-fluorophenyl)-6-(4-(2-(9H-fluoren-9-ylidene)-acetamido)butylamino)-nicotinamide 
• 1195760-17-8 N-(2-amino-4-fluorophenyl)-6-(3-(2-(9H-fluoren-9-ylidene)-acetamido)propylamino)-nicotinamide 
• 1195760-15-6 N-(2-amino-4-fluorophenyl)-6-(2-(2-(9H-fluoren-9-ylidene)-acetamido)ethylamino)-nicotinamide 
• 1195760-13-4 N-(2-aminophenyl)-6-(4-(2-(9H-fluoren-9-ylidene)acetamido)-butylamino)nicotinamide 
• 1195760-11-2 N-(2-aminophenyl)-6-(3-(2-(9H-fluoren-9-ylidene)acetamido)-propylamino)nicotinamide 

Relevant articles and documents

UREA DERIVATIVES USEFUL AS CALCIUM RECEPTOR MODULATORS

The present invention provides compounds of formula (I): in which Y is oxygen or sulphur; R1 and R”1 are optionally substituted aryl, heteroaryl or a fused ring structure, R2and R'2 are each H, or optionally substituted alkyl, alkylaminoalkyl or dialkylaminoalkyl, or R2 and R'2 and their N form a saturated or unsaturated optionally substituted heterocycle, R3 represents a group of formula -(CH2)P-Ar-Rn, wherein p is 0 or 1 and, when p is 1, is optionally substituted, Ar is aryl or heteroaryl, and each R is H, halogen; hydroxyl; trifiuoromethyl; linear and branched alkyl, alkenyl, alkynyl, and alkoxyl groups, all optionally further substituted by one or more of hydroxy groups, halogen atoms, alkoxy groups, amino groups, and alkylthio groups; linear and branched alkoxyl groups; linear and branched thioalkyl groups; aryl groups; aralkyl groups; aralkoxy groups; aryloxy groups; perfluoroalkyl; -CN; -NR4R5, -C(=X)NR4R5,-O-C(=X)NR4R5, -SO2NR4R5, - Alk-NR4R5, -NZC(=X)(NH)qR6, -Alk-NZC(=X)(NH)qR6, -C(=X)R6, -Alk-C(=X)(NH)qR6, -NHSO2R7, -SO2R7, -SOR7, -SR7, or is a saturated or unsaturated heterocyclyl group, and salts and esters thereof, are useful in the treatment of conditions susceptible to modulating ion channels, to a process for their preparation, their application by way of medicaments, and to pharmaceutical compositions containing them.

A CONVENIENT PREPARATION OF 9H-FLUORENE-9-ACETIC ACID

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