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α-(15)N-phenyl azide is a chemical compound with the molecular formula C6H5N315N, where the 15N isotope of nitrogen is incorporated into the molecule. α-(15)N-phenyl azide is a derivative of phenyl azide, which is an aromatic azide, and is characterized by the presence of a phenyl group (C6H5) attached to an azide group (N3). The incorporation of the 15N isotope can be used for various purposes, such as studying the chemical reactivity and dynamics of the molecule, as well as in isotopic labeling for analytical and research purposes. α-(15)N-phenyl azide is typically synthesized through the reaction of 15N-labeled aniline with sodium azide, and it is used in chemical research, particularly in the field of organic chemistry and as a precursor for the synthesis of other 15N-labeled compounds.

70615-33-7

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70615-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70615-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,1 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70615-33:
(7*7)+(6*0)+(5*6)+(4*1)+(3*5)+(2*3)+(1*3)=107
107 % 10 = 7
So 70615-33-7 is a valid CAS Registry Number.

70615-33-7Upstream product

70615-33-7Relevant academic research and scientific papers

The Infrared spectrum, light-induced infrared linear dichroism and conformational analysis of phenyl azide in solid nitrogen at 12 K

Dunkin, Ian R.

, p. 649 - 656 (1986)

Phenyl azide (PhN3) and an isotopic mixture of Ph(14)N3 and Ph(15)N(14)N(14)N were isolated in N2 matrices at 12 K, and i.r. spectra in the range 4000-400 cm-1 were recorded.Photolysis of matrix-isolated PhN3 with plane-polarized light generate

Laser-Induced Fluorescence Spectrum of the Cyanocyclopentadienyl Radical. A Band System Long Attributed to Triplet Phenylnitrene

Cullin, David W.,Soundararajan, N.,Platz, Matthew S.,Miller, Terry A.

, p. 8890 - 8896 (1990)

The UV electronic spectrum long attributed to the triplet phenylnitrene intermediate has been reexamined.A variety of evidence strongly indicates that the true carrier of this spectrum is not phenylnitrene, but the cyanocyclopentadienyl radical.This evide

Flow synthesis of organic azides and the multistep synthesis of imines and amines using a new monolithic triphenylphosphine reagent

Smith, Catherine J.,Smith, Christopher D.,Nikbin, Nikzad,Ley, Steven V.,Baxendale, Ian R.

supporting information; experimental part, p. 1927 - 1937 (2011/04/21)

Here we describe general flow processes for the synthesis of alkyl and aryl azides, and the development of a new monolithic triphenylphosphine reagent, which provides a convenient format for the use of this versatile reagent in flow. The utility of these new tools was demonstrated by their application to a flow Staudinger aza-Wittig reaction sequence. Finally, a multistep aza-Wittig, reduction and purification flow process was designed, allowing access to amine products in an automated fashion.

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