893447-53-5 Usage
Indazole derivative
It is a chemical compound derived from the indazole structure, which is a five-membered aromatic heterocyclic ring system containing three nitrogen atoms.
Carbonitrile functional group
The presence of a cyano group (C≡N) in its structure, which imparts unique chemical properties and reactivity to the compound.
Diverse reactivity
1H-Indazole-1-carbonitrile can undergo various chemical reactions, making it a versatile building block in the synthesis of different compounds.
Structural versatility
The compound's structure allows for modifications and substitutions, enabling the creation of a wide range of derivatives with different properties and applications.
Pharmaceutical and agrochemical synthesis
Due to its reactivity and structural versatility, 1H-Indazole-1-carbonitrile is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals.
Potential biological activities
1H-Indazole-1-carbonitrile has been studied for its potential antifungal, antibacterial, and anticancer properties, indicating its potential use in medicine.
Applications in medicine, agriculture, and materials science
The compound's unique properties and potential applications make it an important and versatile chemical in various fields, including medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 893447-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,4,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 893447-53:
(8*8)+(7*9)+(6*3)+(5*4)+(4*4)+(3*7)+(2*5)+(1*3)=215
215 % 10 = 5
So 893447-53-5 is a valid CAS Registry Number.
893447-53-5Relevant articles and documents
Nitrenes, diradicals, and ylides. Ring expansion and ring opening in 2-quinazolylnitrenes
Kvaskoff, David,Bednarek, Pawel,George, Lisa,Waich, Kerstin,Wentrup, Curt
, p. 4049 - 4058 (2007/10/03)
Tetrazolo[1,5-a]quinazoline (9) is converted to 2-azidoquinazoline (10) on sublimation at 200 °C and above, and the azide-tetrazole equilibrium is governed by entropy. 2-Quinazolylnitrenes 11 and 27 and/ or their ring expansion products 14 and 29 can unde
