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2-Ethyl-3-phenyl-oxaziridine is a chemical compound with the molecular formula C11H13NO. It is a heterocyclic compound, specifically an oxaziridine, which is a three-membered ring containing one oxygen and one nitrogen atom. 2-ethyl-3-phenyl-oxaziridine is characterized by the presence of an ethyl group (C2H5) at the 2-position and a phenyl group (C6H5) at the 3-position. 2-Ethyl-3-phenyl-oxaziridine is an important intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It is known for its high reactivity due to the strained three-membered ring, which makes it a valuable tool in the formation of carbon-carbon and carbon-heteroatom bonds. The compound is typically synthesized through the reaction of α-phenylethylamine with an appropriate oxidizing agent, such as peracetic acid or m-chloroperbenzoic acid.

7771-15-5

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7771-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7771-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7771-15:
(6*7)+(5*7)+(4*7)+(3*1)+(2*1)+(1*5)=115
115 % 10 = 5
So 7771-15-5 is a valid CAS Registry Number.

7771-15-5Upstream product

7771-15-5Relevant academic research and scientific papers

Synthesis of stable isoxazolines by [3+2] cycloaddition of oxaziridines with alkynes

Fabio, Marilena,Ronzini, Ludovico,Troisi, Luigino

, p. 4979 - 4984 (2008/09/21)

N-Alkyl substituted oxaziridines undergo a [3+2] cycloaddition reaction with a variety of terminal alkynes to give the product isoxazolines, whose stability appears to depend on the electronic properties of the groups on the C-3 and C-5 positions. The presence of an electron withdrawing group on C-5 and/or an electron donating group on C-3 causes isomerization of the isoxazolines to β-amino enones.

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