151526-73-7 Usage
Stereochemistry
2S,3S configuration This refers to the specific arrangement of atoms around the stereocenters in the molecule, which can affect the properties and reactivity of the compound.
Aziridine-based compound
A diester of aziridinecarboxylic acid The compound is derived from aziridine, a small nitrogen-containing ring structure, and has two ester functional groups attached to the aziridine ring.
Organic synthesis intermediate
Commonly used as a building block or intermediate This compound can be used in various chemical reactions to form different products, making it a valuable tool in organic synthesis.
Reactivity
Can undergo various reactions Due to its unique structure and functional groups, the compound can participate in a range of chemical reactions, allowing for the synthesis of diverse products.
Potential pharmacological or biological activities
Of interest in medicinal chemistry and drug discovery Studies have suggested that this compound may have biological or pharmacological properties, making it a potential candidate for further research in drug development and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 151526-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,2 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151526-73:
(8*1)+(7*5)+(6*1)+(5*5)+(4*2)+(3*6)+(2*7)+(1*3)=117
117 % 10 = 7
So 151526-73-7 is a valid CAS Registry Number.
151526-73-7Relevant articles and documents
An improved synthesis of aziridine-2,3-dicarboxylates via azido alcohols - Epimerization studies
Breuning, Alexander,Vicik, Radim,Schirmeister, Tanja
, p. 3301 - 3312 (2007/10/03)
The reasons for epimerization of 3-azido-2-hydroxysuccinates observed during the ring opening of epoxides or cyclic sulfites with sodium azide is now clarified. It is caused by the high acidity of the proton at the 3-position. This is proven by a proton deuterium exchange in assays with either D 2O or DCl containing solvents. The anti-3-azido-2-hydroxysuccinates serve as intermediates for enantiomerically pure trans-aziridine-2,3- dicarboxylates for which an optimized synthetic pathway is presented. The first example of an enantiomerically pure mixed diester of the aziridine-2,3- dicarboxylic acid the synthesis of the allyl ethyl ester is reported herein.
