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1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE is a tetraazaparacyclophane derivative, characterized by its unique cyclic structure and nitrogen-containing functional groups. It is commonly substituted to enhance its water solubility, which allows for the formation of inclusion complexes. This property makes it a versatile compound with potential applications in various fields.

74043-83-7

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74043-83-7 Usage

Uses

Used in Chemical Synthesis:
1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE is used as a building block in the synthesis of various complex organic molecules. Its unique cyclic structure and nitrogen-containing functional groups make it a valuable component in the creation of novel compounds with specific properties and applications.
Used in Supramolecular Chemistry:
1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE is used as a host molecule in supramolecular chemistry for the formation of inclusion complexes. Its enhanced water solubility allows for the encapsulation of guest molecules, leading to the development of new materials with unique properties and potential applications in various fields.
Used in Pharmaceutical Industry:
1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE is used as a potential drug candidate or as a component in drug delivery systems. Its ability to form inclusion complexes can be utilized to improve the solubility, stability, and bioavailability of pharmaceutical compounds, leading to enhanced therapeutic effects.
Used in Environmental Applications:
1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE can be used in environmental applications, such as the removal of pollutants or the capture of greenhouse gases. Its ability to form inclusion complexes can be exploited to selectively bind and remove specific contaminants from the environment, contributing to a cleaner and more sustainable future.
Used in Materials Science:
1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE can be used in the development of new materials with unique properties, such as stimuli-responsive materials, sensors, or catalysts. Its ability to form inclusion complexes can be utilized to create materials with specific binding properties, leading to innovative applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 74043-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,4 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74043-83:
(7*7)+(6*4)+(5*0)+(4*4)+(3*3)+(2*8)+(1*3)=117
117 % 10 = 7
So 74043-83-7 is a valid CAS Registry Number.

74043-83-7SDS

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 1,6,20,25-Tetraaza[6.1.6.1]paracyclophane

1.2 Other means of identification

Product number -
Other names 1,6,20,25-TETRAAZA[6.1.6.1]PARACYCLOPHANE

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:74043-83-7 SDS

74043-83-7Relevant academic research and scientific papers

Biomimetic Studies Using Artificial Systems. 3. Design, Synthesis, and Inclusion Complex Forming Ability of a Novel Water-Soluble Paracyclophane Possessing Diphenylmethane Skeletons

Odashima, Kazunori,Itai, Akiko,Iitaka, Yoichi,Koga, Kenji

, p. 4478 - 4484 (2007/10/02)

A novel water-soluble paracyclophane, CP44 (1), was designed and synthesized as a host molecule possessing a hydrophobic cavity to capture organic guests in water.X-ray crystallographic study revealed the formation of 1:1 inclusion complex, and not a simp

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