40711-15-7 Usage
Physical state
Highly reactive and volatile liquid
Odor
Faint
Usage
Commonly used as a reagent in organic synthesis
Reactivity
Known for its ability to undergo ring-opening reactions
Applications
Valuable tool for creating functionalized molecules
Pharmaceutical and agrochemical synthesis
Used in the synthesis of pharmaceuticals and agrochemicals due to its unique reactivity and stability under certain reaction conditions
Safety precautions
Handle with caution due to potential for explosive decomposition when heated or exposed to strong acids or bases
Check Digit Verification of cas no
The CAS Registry Mumber 40711-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,1 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40711-15:
(7*4)+(6*0)+(5*7)+(4*1)+(3*1)+(2*1)+(1*5)=77
77 % 10 = 7
So 40711-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2/c1-4(2)5-6(4)3/h5H,1-3H3
40711-15-7Relevant articles and documents
THE ROLE OF pH IN THE SYNTHESIS OF DIAZIRIDINES
Kuznetsov, V. V.,Makhova, N. N.,Strelenko, Yu. A.,Khmel'nitskii, L. I.
, p. 2496 - 2505 (2007/10/02)
The greatest yield in the synthesis of diaziridines from carbonyl compounds, amines, and aminating reagents in water is achieved at a specific pH, which shifts to less alkaline values with increasing -I effect of the substituents in the carbonyl compound and with increasing pKBH+ value of the amine.The role of pH is related to the conditions for the generation of an immonium from the intermediate α-aminocarbinol.The nuclear Overhauser effect was used to determine the orientation of the substituents in several diastereomers of the dialkyldiaziridines obtained.
