71367-28-7

Basic information

• Product Name: 3-(10-(2-CARBOXY-ETHYL)-ANTHRACEN-9-YL)-PROPIONIC ACID
• Synonyms: 3-(10-(2-CARBOXY-ETHYL)-ANTHRACEN-9-YL)-PROPIONIC ACID;9,10-ANTHRACENEDIPROPIONIC ACID);9,10-Anthracenedipropanoicacid;3,3'-(Anthracene-9,10-diyl)dipropanoic acid
• CAS NO: 71367-28-7
• Molecular Formula: C₂₀H₁₈O₄
• Molecular Weight: 322.35452
• Mol File: 71367-28-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 244 °C
• Boiling Point: 596.0±30.0 °C(Predicted)
• Appearance: /
• Density: 1.312±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.29±0.10(Predicted)
• CAS DataBase Reference: 3-(10-(2-CARBOXY-ETHYL)-ANTHRACEN-9-YL)-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(10-(2-CARBOXY-ETHYL)-ANTHRACEN-9-YL)-PROPIONIC ACID(71367-28-7)
• EPA Substance Registry System: 3-(10-(2-CARBOXY-ETHYL)-ANTHRACEN-9-YL)-PROPIONIC ACID(71367-28-7)

Safety Data

• Hazardous Substances Data: 71367-28-7(Hazardous Substances Data)

Usage

General Description

3-(10-(2-Carboxy-Ethyl)-Anthracen-9-Yl)-Propionic Acid is a chemical compound likely used in the field of organic chemistry and in the production of various materials or pharmaceuticals due to its anthracene backbone. Anthracene is a solid polycyclic aromatic hydrocarbon consisting of three fused benzene rings. This makes it part of important compounds such as dyes, pharmaceuticals, and even explosives. Additionally, the presence of propionic acid can increase its reactivity. However, specific information about this compound's properties, usages, safety, or potential health effects isn't readily available, indicating that it may not be a widely used or well-studied compound. It is advised to handle all chemicals with care, ensuring appropriate safety precautions are in place because the properties and potential hazards of this particular compound aren't fully understood.

Upstream product

• 1225023-89-1 di-tert-butyl 3,3'-(anthracene-9,10-diyl)dipropionate 
• 120-12-7 anthracene 
• 523-27-3 9,10-Dibromoanthracene 
• 1225023-88-0 di-tert-butyl 3,3'-(9,10-anthracenediyl)bis(2-propenoate) 
• 10387-13-0 9,1-bis(chloromethyl)anthracene 
• 307554-61-6 9,10-bis<<2,2-di(ethoxycarbonyl)>ethyl>anthracene 
• 34373-96-1 9,10-dibromomethylanthracene 
• 781-43-1 9,10-dimethylanthracene 
• 307554-62-7 α,α'-(anthracene-9,10-diyl)bis(methylmalonic)acid 

Downstream Products

• 916500-86-2 N,N'-di(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide 
• 1225023-87-9 9,10-dihydro-N-(4-nitrophenyl)-9,10-(epoxyimino)-11-carbamylanthracene-9,10-dipropanoic acid 
• 1225023-90-4 (S,S)-di-tert-butyl 2-(3-{10-[2-(1-tert-butoxycarbonylmethyl-2-isopropoxy-ethylcarbamoyl)ethyl]anthracen-9-yl}propionylamino)butanedioate 
• 97760-36-6 3,14-dioxo-7,10,19,22-tetraoxa-4,13-diaza<16,8^4,13>(9,10)-anthracenophane 
• 97760-38-8 7,10,19,22-tetraoxa-4,13-diaza<16,8^4,13>(9,10)anthracenophane 
• 132056-51-0 diethyl 9,10-anthracenedipropionate 
• 109399-65-7 9,10-Bis-<2-carboxy-aethyl>-9,10-dihydro-anthracen 
• 97760-33-3 9,10-anthracenedipropionyl dichloride 

Relevant articles and documents

Photosensitizing properties of hollow microcapsules built by multilayer self-assembly of poly(allylamine hydrochloride) modified with rose Bengal

A polymeric photosensitizer based on poly(allylamine hydrochloride) (PAH) and rose Bengal (RB) was synthesized. The modified polycation PAH-RB was demonstrated to be suitable for construction of microcapsules via a layer-by-layer (LbL) assembly technique, using sodium poly(styrene sulfonate) (PSS) as counter-polyelectrolyte and CaCO3 microcrystals as templates. After CaCO3 core removal, a stable suspension of hollow microcapsules with shells incorporating RB (HM-RB) was obtained. The spectroscopic and photophysical behavior of both PAH-RB and HM-RB in aqueous environments were studied and described in terms of dye-dye interactions and dye hydrophobicity. Only HM-RB was able to generate singlet molecular oxygen with similar efficiency to free RB in air-saturated solutions upon green light irradiation. In order to explore possible practical applications as a supramolecular photosensitizer, experiments of HM-RB irradiation in the presence of chemically and biologically relevant target molecules were carried out. It was observed that is possible to use visible light to initiate the photooxidation of biological compounds in water, with many interesting advantages compared to low-molecular-weight photosensitizers such as an enhancement of the photosensitizing effect, due to a significant reduction of dye-dye interaction, or improved reuse given the straightforward size-based separation from the reaction mixture without loss of efficiency.

Synthetic β-Cyclodextrin Dimers for Squaraine Binding: Effect of Host Architecture on Photophysical Properties, Aggregate Formation and Chemical Reactivity

Reported herein is the synthesis and application of three novel β-cyclodextrin dimer hosts for the complexation of near infrared (NIR) squaraine dyes in aqueous solution. A series of eight different N-substituted N-methyl anilino squaraine dyes with variable terminal groups are investigated, with an optimal n-hexyl-substituted squaraine guest demonstrating binding constants orders of magnitude higher than the other squaraine–host combinations and comparable to literature-reported systems. Moreover, hydrophobic complexation of the squaraine dyes with the β-cyclodextrin dimer hosts causes drastic changes in the squaraine's photophysical properties, propensity for aggregation and susceptibility to hydrolytic decay.

Alternative photoinduced release of HNO or NO from an acyl nitroso compound, depending on environmental polarity

A hydrophilic hetero-Diels-Alder cycloadduct was synthesized as a novel photocontrollable donor of reactive nitrogen species. Production of either nitric oxide (NO) or nitroxyl (HNO) was photoinduced from this compound, depending on the environmental polarity.