124014-00-2

Basic information

• Product Name: 5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL 9&
• Synonyms: 5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL 9&;5-(3-Chloro-4-methoxyphenyl)furfural 97%;5-(3-chloro-4-methoxyphenyl)furan-2-carbaldehyde
• CAS NO: 124014-00-2
• Molecular Formula: C₁₂H₉ClO₃
• Molecular Weight: 236.653
• Product Categories: API intermediates;Building Blocks;Furans;FuransHeterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks
• Mol File: 124014-00-2.mol
• Article Data: 2

Chemical Properties

• Melting Point: 128-130 °C(lit.)
• Boiling Point: 387°C at 760 mmHg
• Flash Point: 187.8°C
• Appearance: /
• Density: 1.278g/cm³
• Vapor Pressure: 3.41E-06mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: 5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL 9&(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL 9&(124014-00-2)
• EPA Substance Registry System: 5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL 9&(124014-00-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 124014-00-2(Hazardous Substances Data)

Usage

General Description

5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL is a chemical compound with the formula C11H7ClO3. It is a furan derivative that contains a furan ring with a 3-chloro-4-methoxyphenyl group attached to it. 5-(3-CHLORO-4-METHOXYPHENYL)FURFURAL 9& is commonly used in organic synthesis and has potential applications in the pharmaceutical and agrochemical industries. It can be used as a building block for the synthesis of other organic compounds and has been studied for its potential biological activities. However, further research is needed to fully understand its properties and potential uses.

InChI:InChI=1/C12H9ClO3/c1-15-12-4-2-8(6-10(12)13)11-5-3-9(7-14)16-11/h2-7H,1H3

Upstream product

• 98-01-1 furfural 
• 5345-54-0 3-chloro-4-methoxyaniline 
• 1899-24-7 5-bromo-2-furancarboxaldehyde 
• 175883-60-0 3-chloro-4-methoxyphenylboronic acid 

Downstream Products

• 443289-30-3 [5-(3-chloro-4-methoxyphenyl)furan-2-yl]methanol 
• 1210046-68-6 (R)-1-(5-(3-chloro-4-methoxyphenyl)furan-2-yl)-2,2-dimethylbut-3-en-1-ol 
• 1210046-61-9 (R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]but-3-en-1-ol 
• 1210046-66-4 (1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol 
• 1392419-43-0 C₂₂H₁₄ClNO₆ 
• 1392418-55-1 C₂₈H₁₇ClF₃NO₅ 
• 1392419-52-1 C₂₂H₁₃ClF₃NO₄ 

Relevant articles and documents

Red- to NIR-Emitting, BODIPY-Based, K+-Selective Fluoroionophores and Sensing Materials

Optical sensing materials for the selective measurement of potassium ions (K+) in water are presented. The indicator dyes are based on an aza-crown ether as a receptor and borondipyrromethenes (BODIPY) dyes as fluorophores. Fluorescence enhancement is caused by the reduction of photoinduced electron transfer (PET) upon complexation with K+ ions. The family of new indicators possesses tuneable optical properties (green to red excitation, red to NIR emission) and PET efficiencies. They exhibit high brightness with quantum yields between 0.20 and 0.47 in the “on” state and a molar absorption coefficient between 30 000 and 290 000 m?1 cm?1. The new indicator dyes are immobilized in biocompatible hydrogel matrices to obtain stable nonleaching and fast responding (t90 ≈ 10 s) sensing materials for continuous measurements of potassium. They are realized in various formats such as planar optodes, fiber-optic sensors, and water-dispersible polymer-based nanoparticles. Apart from fluorescence intensity measurements, self-referenced read-out of fluorescence decay time is demonstrated. All sensor materials display a high K+/Na+ selectivity and are not influenced by pH within the physiologically relevant range. Practical applicability of the materials is emphasized by application of a fiber-optic sensor to quantification of K+ in serum, which shows excellent correlation with the reference measurements.