125187-91-9 Usage
Derivative of pyrrole
heterocyclic aromatic organic compound 1H-Pyrrole, 1-(2-azidophenyl)is derived from pyrrole, which is a heterocyclic (containing atoms of different elements) aromatic compound consisting of a ring with alternating single and double bonds.
Azido group attachment
phenyl ring The azido group (N3) is attached to the phenyl ring (a benzene ring with a hydrogen atom replaced by an azide group) in the compound, making it more reactive.
Building block in organic synthesis
1H-Pyrrole, 1-(2-azidophenyl)is commonly used as a building block in organic synthesis, meaning it can be used to create more complex molecules through chemical reactions.
Potential precursor for new materials and pharmaceuticals
1H-Pyrrole, 1-(2-azidophenyl)- is of interest for its potential use as a starting material in the synthesis of new materials and pharmaceuticals, due to its unique structure and reactivity.
Reactive azido group
click chemistry and other chemical reactions The azido group in 1H-Pyrrole, 1-(2-azidophenyl)makes it suitable for various chemical reactions, including click chemistry, a type of reaction used to form carbon-heteroatom bonds.
Hazardous properties
explosive under certain conditions Azides, including the azido group in 1H-Pyrrole, 1-(2-azidophenyl)-, are known to be explosive under specific conditions, so it is important to handle 1H-Pyrrole, 1-(2-azidophenyl)with care to avoid any hazardous situations.
Check Digit Verification of cas no
The CAS Registry Mumber 125187-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,8 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125187-91:
(8*1)+(7*2)+(6*5)+(5*1)+(4*8)+(3*7)+(2*9)+(1*1)=129
129 % 10 = 9
So 125187-91-9 is a valid CAS Registry Number.
125187-91-9Relevant academic research and scientific papers
Tandem C-2 functionalization-intramolecular Azide-Alkyne 1,3-Dipolar Cycloaddition reaction: A convenient route to highly diversified 9H-Benzo[b]pyrrolo[1,2-g][1,2,3]triazolo[1,5-d][1,4]diazepines
Hussain, Mohd. Kamil,Ansari, Mohd. Imran,Kant, Ruchir,Hajela, Kanchan
supporting information, p. 560 - 563 (2014/04/03)
An efficient diversity-oriented synthetic approach to annulated 9H-benzo[b]pyrrolo[1,2-g][1,2,3]- triazolo[1,5-d][1,4]diazepines has been developed using a Sc(OTf)3-catalyzed two-component tandem C-2 functionalization- intramolecular azide-alky
New methodology for the preparation of pyrrole and indole derivatives via iminophosphoranes:synthesis of pyrrolo[1,2-a]quinoxalines, indolo[3,2-c]quinolines and indolo[1,2-c]quinazolines
Molina, Pedro,Alajarin, Mateo,Vidal, Angel
, p. 1063 - 1078 (2007/10/02)
The aza-Wittig reaction of iminophosphorane N-[o-(triphenylphosphoranylidene)amino]-phenyl pyrrole 4 with heterocumulenes leads to functionalized pyrrolo[1,2-a]quinoxalines. Iminophosphorane 19, derived from 2-(o-amino)phenyl indole, reacts under mild con
ortho-PYRROLYLPHENYL HETEROCUMULENES: PREPARATION AND CYCLIZATION TO FUSED PYRROLES
Molina, Pedro,Alajarin, Mateo,Vidal, Angel
, p. 2847 - 2850 (2007/10/02)
The aza-Wittig reaction of iminophosphoranes derived from o-(1-pyrrolyl)phenyl azide and 2-(o-aminophenyl)indole with isocyanates, isothiocyanates, carbon dioxide or carbon disulfide, lead to functionalized pyrroloquinoxalines and 11H-indolo
