16719-56-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C) atoms, 16 hydrogen (H) atoms, 1 iodine (I) atom, and 2 nitrogen (N) atoms.
Explanation
The structure describes the arrangement of atoms and the type of chemical bonds between them. This compound has a naphthalene ring with a tetrahydronaphthalen-1-yl group attached to the 1-position, an iodine atom at the 2-position, and a triaza-1,2-dien-2-ium group at the 1-position.
Explanation
The compound belongs to the tetrahydronaphthalene family, which is a group of organic compounds derived from naphthalene by the addition of hydrogen atoms to the molecule.
Explanation
The compound is classified as a quaternary ammonium compound because it contains a positively charged nitrogen atom (quaternary ammonium cation) that is bonded to four organic groups.
Explanation
The triaza-1,2-dien-2-ium group is a heterocyclic compound containing three nitrogen atoms and is attached to the naphthalene ring, contributing to the compound's reactivity and potential applications.
Explanation
The compound can be used as a building block in organic synthesis, which is the process of creating new organic compounds by forming or breaking chemical bonds.
Explanation
Due to its structural features, the compound has the potential to be used in the development of pharmaceuticals and medicines. However, more research is needed to fully understand its properties and potential uses.
Explanation
While the compound has potential applications in various fields, more studies are required to fully comprehend its properties, reactivity, and potential uses in pharmaceuticals, materials science, and other areas.
Structure
1-(2-iodo-1,2,3,4-tetrahydronaphthalen-1-yl)triaza-1,2-dien-2-ium
Family
Tetrahydronaphthalene
Class
Quaternary ammonium compounds
Iodine atom
Present
Triaza-1,2-dien-2-ium group
Attached to the naphthalene ring
Application
Building block in organic synthesis
Potential use
Pharmaceutical and medicinal applications
Further studies needed
To understand properties and potential uses
Check Digit Verification of cas no
The CAS Registry Mumber 16719-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,1 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16719-56:
(7*1)+(6*6)+(5*7)+(4*1)+(3*9)+(2*5)+(1*6)=125
125 % 10 = 5
So 16719-56-5 is a valid CAS Registry Number.
16719-56-5Relevant articles and documents
Photoswitchable Regiodivergent Azidation of Olefins with Sulfonium Iodate(I) Reagent
Rao, Dodla S.,Reddy, Thurpu R.,Gurawa, Aakanksha,Kumar, Manoj,Kashyap, Sudhir
, p. 9990 - 9994 (2019)
Photoswitchable strategy for selective azidation of structurally diverse olefins under transition-metal-free conditions is reported. The unprecedented reactivity of trimethylsulfonium [bis(azido)iodate(I)] species under visible light allows radical azidooxygenation of the C═C πbond with distinctive selectivity. In the absence of visible light, the reaction proceeds through an ionic intermediate which led to complementary regioselectivity to provide α-alkyl azides. Mechanistic studies reveal that light-controlled regiodivergent azidation involving radical or an ionic pathway can be accomplished with exclusive regioselectivity.
