Welcome to LookChem.com Sign In|Join Free
  • or
4'-Formylbenzo-18-crown-6-ether is a versatile chemical compound that features a benzene ring with a formyl group and an 18-crown-6-ether moiety. This unique structure endows it with the capability to engage in selective complexation with metal ions, particularly alkali and alkaline-earth metal ions. It is renowned for its stable complex formation with potassium and sodium ions, which positions it as a significant player in ion recognition and separation chemistry. 4'-Formylbenzo-18-crown 6-ether's distinctive attributes render it beneficial across a spectrum of disciplines, including analytical chemistry, environmental science, and material science. Furthermore, 4'-Formylbenzo-18-crown-6-ether holds promise for exploration in supramolecular chemistry and pharmaceutical research.

60835-74-7

Post Buying Request

60835-74-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

60835-74-7 Usage

Uses

Used in Coordination Chemistry:
4'-Formylbenzo-18-crown-6-ether serves as a ligand in coordination chemistry, where it plays a crucial role in the selective complexation of metal ions. Its ability to form stable complexes with potassium and sodium ions is particularly noteworthy, facilitating its use in various chemical processes and reactions.
Used in Ion Recognition and Separation Chemistry:
In the field of ion recognition and separation chemistry, 4'-Formylbenzo-18-crown-6-ether is utilized for its selective binding properties with specific metal ions. This selective complexation is instrumental in processes that require the separation or identification of particular ions within a mixture.
Used in Analytical Chemistry:
4'-Formylbenzo-18-crown-6-ether is applied in analytical chemistry to enhance the detection and quantification of metal ions. Its unique structure allows for the development of sensitive and selective analytical methods, improving the accuracy and efficiency of ion analysis.
Used in Environmental Science:
In environmental science, 4'-Formylbenzo-18-crown-6-ether is employed for its potential in metal ion remediation and environmental monitoring. Its ability to selectively bind with metal ions can be harnessed to remove or detect contaminants in various environmental matrices.
Used in Material Science:
4'-Formylbenzo-18-crown 6-ether's properties make it a valuable component in the development of new materials with specific functionalities. Its use in material science can lead to the creation of materials with tailored properties for various applications, such as sensors, catalysts, or advanced materials with unique structural characteristics.
Used in Supramolecular Chemistry:
4'-Formylbenzo-18-crown-6-ether holds potential in supramolecular chemistry, where it can be used to construct complex molecular assemblies and architectures. Its ability to form stable complexes with metal ions contributes to the development of supramolecular systems with novel functions and properties.
Used in Pharmaceutical Research:
In pharmaceutical research, 4'-Formylbenzo-18-crown-6-ether may be explored for its potential applications in drug design and delivery. Its metal ion binding properties could be leveraged to develop new drug candidates or improve the efficacy and targeting of existing pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 60835-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,3 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60835-74:
(7*6)+(6*0)+(5*8)+(4*3)+(3*5)+(2*7)+(1*4)=127
127 % 10 = 7
So 60835-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H24O7/c18-14-15-1-2-16-17(13-15)24-12-10-22-8-6-20-4-3-19-5-7-21-9-11-23-16/h1-2,13-14H,3-12H2

60835-74-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5,8,11,14,17-hexaoxabicyclo[16.4.0]docosa-1(18),19,21-triene-20-carbaldehyde

1.2 Other means of identification

Product number -
Other names F0451

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60835-74-7 SDS

60835-74-7Relevant academic research and scientific papers

Synthesis of formyl derivatives of benzocrown ethers containing N, S, and O heteroatoms in the macrocycle

Gromov, S. P.,Fedorova, O. A.,Vedernikov, A. I.,Samoshin, V. V.,Zefirov, N. S.,Alfimov, M. V.

, p. 116 - 123 (2007/10/02)

A method for the synthesis of 4'-bromobenzodithia-15(18)-crown-5(6) and 4'-bromobenzodiaza-15(18)-crown-5(6) by condensation of 3,4-di(2'-haloethoxy)bromobenzene with polyoxaalkanes containing terminal SH or NHMe groups was suggested.The method for the synthesis of formyl derivatives of benzocrowns containing N, S, and O heteroatoms in the macrocycle based on the metallation of appropriate bromo derivatives with BunLi followed by treatment of the resulting organolithium intermediates with DMF was developed.Oximes and semicarbazones of benzaldehydes containing a crown ether fragment were obtained, and their transformation into the original aldehydes by treatment with KNO2 in an acid medium was studied. - Key words: 4'-bromobenzocrowns, synthesis, metallation; 4'-formylbenzocrown ethers; semicarbazones and oximes of 4'-formylbenzocrown ethers.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 60835-74-7