14141-68-5 Usage
Chemical structure
1,2,4,5-tetrazine-3,6-diylbis[(4-methoxyphenyl)methanol] is a complex organic compound with a tetrazine backbone and two 4-methoxyphenylmethanol substituents.
Application
It is commonly used in the field of medicinal chemistry and pharmaceutical research, particularly in the development of novel drugs and pharmaceuticals.
Chemical properties
The compound possesses unique chemical properties and is known for its ability to form stable complexes with various ligands and biomolecules.
Versatile nature
Its versatile nature makes it a valuable tool in drug discovery and development, as well as in the study of molecular interactions and biological processes.
Potential applications
It has potential applications in the fields of materials science and organic synthesis due to its interesting structure and reactivity.
Stability
The compound is known for its ability to form stable complexes, which is a desirable property in the development of drugs and pharmaceuticals.
Reactivity
The compound's interesting structure and reactivity make it a valuable tool in organic synthesis and materials science.
Molecular interactions
The compound is known for its ability to interact with various biomolecules, which is important in the study of biological processes and drug discovery.
Biological processes
The compound's ability to interact with biomolecules makes it a useful tool in the study of biological processes.
Drug discovery
The compound's unique properties and versatility make it a valuable tool in the development of novel drugs and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 14141-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,4 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14141-68:
(7*1)+(6*4)+(5*1)+(4*4)+(3*1)+(2*6)+(1*8)=75
75 % 10 = 5
So 14141-68-5 is a valid CAS Registry Number.
14141-68-5Relevant articles and documents
An Investigation into the Mechanism of Formation of Oxadiazoles and Arylidenehydrazides from the Action of Methanolic Potassium Hydroxide on 1,4-Dihydro-s-tetrazines.
Hunter, Daniel,Neilson, Douglas G.
, p. 1081 - 1086 (2007/10/02)
3,6-Diaryl- and 3,6-dibenzyl-1,4-dihydro-s-tetrazines have been shown to be inert to methanolic alkali under nitrogen.Oxadiazoles derived from these substances by the action of alkali in methanol in air result from alkali attack on the tetrazines themselves and not on the reduced derivatives as previously believed. 1,4-Dihydro-3,6-bis(α-hydroxybenzyl)-s-tetrazine is likewise stable to alkali under nitrogen but on exposure to air yields the benzylidene derivative of mandelohydrazide.Mechanisms are here proposed for the formation of the oxadiazoles and hydrazides.
