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3-Azido-1-phenyl-2-propen-1-one is an organic compound with the molecular formula C9H6N3O. It is a derivative of cinnamaldehyde, featuring an azide group (N3) at the 3-position, a phenyl ring at the 1-position, and a carbonyl group at the 2-position. 3-azido-1-phenyl-2-propen-1-one is of interest in chemical research due to its potential applications in the synthesis of various pharmaceuticals and agrochemicals. The azide group can be used as a protecting group or as a source of nitrogen in chemical reactions, while the phenyl ring provides a platform for further functionalization. The compound's reactivity and stability make it a valuable intermediate in organic synthesis, particularly in the preparation of complex molecules with potential biological activity.

1517-00-6

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1517-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1517-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1517-00:
(6*1)+(5*5)+(4*1)+(3*7)+(2*0)+(1*0)=56
56 % 10 = 6
So 1517-00-6 is a valid CAS Registry Number.

1517-00-6Relevant academic research and scientific papers

Cracking under internal pressure: Photodynamic behavior of vinyl azide crystals through N2release

Shields, Dylan J.,Karothu, Durga Prasad,Sambath, Karthik,Ranaweera, Ranaweera A. A. Upul,Schramm, Stefan,Duncan, Alexander,Duncan, Benjamin,Krause, Jeanette A.,Gudmundsdottir, Anna D.,Naumov, Pan?e

, p. 18565 - 18575 (2020/12/01)

When exposed to UV light, single crystals of the vinyl azides 3- azido-1-phenylpropenone (1a), 3-azido-1-(4-methoxyphenyl)propenone (1b), and 3-azido-1-(4-chlorophenyl)propenone (1c) exhibit dramatic mechanical effects by cracking or bending with the release of N2. Mechanistic studies using laser flash photolysis, supported by quantum mechanical calculations, show that each of the vinyl azides degrades through a vinylnitrene intermediate. However, despite having very similar crystal packing motifs, the three compounds exhibit distinct photomechanical responses in bulk crystals. While the crystals of 1a delaminate and release gaseous N2 indiscriminately under paraffin oil, the crystals of 1b and 1c visibly expand, bend, and fracture, mainly along specific crystallographic faces, before releasing N2. The photochemical analysis suggests that the observed expansion is due to internal pressure exerted by the gaseous product in the crystal lattices of these materials. Lattice energy calculations, supported by nanoindentation experiments, show significant differences in the respective lattice energies. The calculations identify critical features in the crystal structures of 1b and 1c where elastic energy accumulates during gas release, which correspond to the direction of the observed cracks. This study highlights the hitherto untapped potential of photochemical gas release to elicit a photomechanical response and motility of photoreactive molecular crystals.

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