174884-21-0

Basic information

• Product Name: 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester
• Synonyms: 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester
• CAS NO: 174884-21-0
• Molecular Formula: C₁₅H₂₀O₅
• Molecular Weight: 280.3163
• Product Categories: Aromatics
• Mol File: 174884-21-0.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• Solubility: Chloroform, Dichloromethane, Dimethyl Formamide
• CAS DataBase Reference: 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester(174884-21-0)
• EPA Substance Registry System: 4-(4-Acetyl-2-Methoxyphenoxy)-butanoic Acid Ethyl Ester(174884-21-0)

Safety Data

• Hazardous Substances Data: 174884-21-0(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

A photolabile linker for the solid-phase synthesis of 4-substituted 1,2,3-triazoles.

Upstream product

• 2969-81-5 Ethyl 4-bromobutyrate 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 

Downstream Products

• 198347-60-3 4-[4-(1-Hydroxy-ethyl)-2-methoxy-phenoxy]-butyric acid ethyl ester 
• 175281-76-2 4-[4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy]butanoic acid 
• 65623-82-7 4-(4-Acetylphenyloxy)butyric acid 
• 1031702-80-3 ethyl 4-(4-acetyl-2-methoxy-5-nitrophenoxy)butanoate 
• 1073426-06-8 ethyl 4-(4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy) butanoate 
• 1285712-73-3 ethyl 4-(4-(1-chloroethyl)-2-methoxy-5-nitrophenoxy)butanoate 
• 1285712-74-4 ethyl 4-(4-(1-azidoethyl)-2-methoxy-5-nitrophenoxy)butanoate 
• 1285712-75-5 4-(4-(1-azidoethyl)-2-methoxy-5-nitrophenoxy)butanoic acid 
• 1091595-09-3 4-(4-(1-(acryloyloxy)ethyl)-2-methoxy-5-nitrophenoxy)butanoic acid 
• 188891-18-1 4-(4-acetyl-2-methoxy-5-nitrophenoxy)butanoic acid 
• 1363555-53-6 C₁₆H₁₈ClNO₇ 
• 162827-97-6 4-[4-(1-aminoethyl)-2-methoxy-5-nitrophenoxy]butyric acid 

Relevant articles and documents

PHOTOPROXIMITY PROFILING OF PROTEIN-PROTEIN INTERACTIONS IN CELLS

Photoactive probes and probe systems for detecting biological interactions are described. The photoactive probes include probes that combine both photocleavable and photoreactive moieties. The photoactive probe systems can include a first probe comprising a photocatalytic group and a second probe comprising a group that can act as a substrate for the reaction catalyzed by the photocatalytic group. The probes and probe systems can also include groups that can specifically bind to a binding partner on a biological entity of interest and a detectable group or a precursor thereof. The probes and probe systems can detect spatiotemporal interactions of proteins or cells. In some embodiments, the interactions can be detected in live cells. Also described are methods of detecting the biological interactions.

PEG-PEI-modified gated N-doped mesoporous carbon nanospheres for pH/NIR light-triggered drug release and cancer phototherapy

A novel hybrid drug carrier has been designed, taking N-doped mesoporous carbon (NMCS) as the core and PEG-PEI as the outer shell. NMCS was functionalized with a photocleavable nitrobenzyl-based linker following a click reaction. Gemcitabine was loaded in

Two Colour Photoflow Chemistry for Macromolecular Design

We report a photochemical flow setup that exploits λ-orthogonal reactions using two different colours of light (λ1=350 nm and λ2=410 nm) in sequential on-line irradiation steps. Critically, both photochemically reactive units (a visi