71331-21-0 Usage
Structure
It is a methylester derivative of aziridinecarboxylicacid, containing a three-membered heterocyclic ring with a nitrogen atom. The 2-propenyl group is attached to the carbon at the 1-position of the aziridine ring.
Applications
Organic Synthesis: Due to its unique reactivity, it can be used as a building block in organic synthesis to create diverse chemical structures.
Pharmaceuticals: It may have applications in pharmaceutical research and drug development.
Materials Science: It might find uses in materials science for the synthesis of novel materials.
Safety Concerns
Toxicity: Aziridine derivatives, including this compound, are known to be toxic.
Carcinogenicity: They also have the potential to be carcinogenic.
Safety Measures
Proper Handling: Handle with caution.
Ventilation: Work in a well-ventilated area to minimize exposure.
Protective Equipment: Wear appropriate protective gear, such as gloves and goggles, when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 71331-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,3 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71331-21:
(7*7)+(6*1)+(5*3)+(4*3)+(3*1)+(2*2)+(1*1)=90
90 % 10 = 0
So 71331-21-0 is a valid CAS Registry Number.
71331-21-0Relevant articles and documents
Stereoselective synthesis of N-alkylaziridines from N-chloroamines
Bew, Sean P.,Hughes,Palmer, Nicholas J.,Savic, Vladimir,Soapi, Katy M.,Wilson, Martin A.
, p. 4338 - 4340 (2007/10/03)
We report the first racemic and stereoselective synthesis of cis- and trans-N-alkylaziridines via N-chloroamines; using this methodology an N-3,4,5-trimethoxybenzylaziridine was synthesised and efficiently cleaved, affording the corresponding NH aziridine
