29200-99-5 Usage
Explanation
The compound is referred to as 2,6-diaziridin-1-ylpyridine due to its structural composition.
Explanation
The term "Pyridazine deriv." is used as a short form or synonym for the compound, indicating its relation to the pyridazine structure.
Explanation
The compound consists of 7 carbon atoms, 7 hydrogen atoms, and 3 nitrogen atoms in its structure.
Explanation
The core structure of the compound is a pyridine ring, with two diaziridinyl groups (a type of nitrogen-containing heterocycle) attached to it at specific positions.
Explanation
2,6-diaziridin-1-ylpyridine is used in the field of organic chemistry as a reagent for specific applications.
Explanation
The compound is used to study biomolecular interactions and structures by forming covalent bonds with proteins and nucleic acids through photochemical reactions.
Explanation
Upon exposure to light, 2,6-diaziridin-1-ylpyridine undergoes photochemical reactions, allowing it to form stable covalent bonds with biomolecules like proteins and nucleic acids.
8. Hazardous and potentially toxic
Explanation
The compound should be handled with caution as it is considered hazardous and potentially toxic, posing risks to human health and the environment.
Synonym
Pyridazine deriv.
Structure
Pyridine ring with two diaziridinyl groups at the 2 and 6 positions
Field of use
Organic chemistry
Applications
Photoaffinity labeling and crosslinking of biomolecules
Photochemical reactions
Forms covalent bonds with proteins and nucleic acids
Check Digit Verification of cas no
The CAS Registry Mumber 29200-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,0 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29200-99:
(7*2)+(6*9)+(5*2)+(4*0)+(3*0)+(2*9)+(1*9)=105
105 % 10 = 5
So 29200-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N3/c1-2-8(11-4-5-11)10-9(3-1)12-6-7-12/h1-3H,4-7H2
29200-99-5Relevant academic research and scientific papers
Witulski, Bernhard,Senft, Stefan,Bonet, Jordi,Jost, Oliver
, p. 243 - 250 (2007)
Studies on the viability of palladium-catalyzed cross-coupling reactions of aryl- or hetaryl bromides with the parent aziridine or azetidine showed that a wide range of N-arylaziridines and N-arylazetidines are accessible by this method. Ring cleavage of the N-arylaziridines or -azetidines thus produced does not occur under the applied reaction conditions. The synthetic utility of the method is illustrated by examples of double N-arylations with either aziridine or azetidine. Georg Thieme Verlag Stuttgart.
