2112-98-3 Usage
Derivative of 1-naphthylamine
1-Naphthalenamine, 8-azidois a modified version of the parent compound 1-naphthylamine, which has a similar structure and some shared properties.
Azido functional group
The azido group is a linear arrangement of three nitrogen atoms (N3) that is present in 1-Naphthalenamine, 8-azido-. This group is responsible for many of the compound's unique properties and reactivity.
Use in organic synthesis
1-Naphthalenamine, 8-azidois commonly used as a reagent for introducing azido groups into organic molecules, which can be important for creating new compounds or modifying existing ones.
Precursor for heterocyclic compounds
This compound can be used as a starting material for the synthesis of various heterocyclic compounds, which are organic compounds containing a ring of atoms with at least one non-carbon atom.
Photoaffinity label in biochemical studies
1-Naphthalenamine, 8-azidocan be used as a photoaffinity label, which helps researchers study the interactions of biomolecules by tagging them with a light-sensitive group that can be activated by exposure to light.
Value in material and pharmaceutical development
The properties and reactivity of 1-Naphthalenamine, 8-azidomake it a useful tool in the development of new materials and pharmaceuticals, as it can be incorporated into a wide range of compounds with different functions.
Potentially explosive
Azido groups are known to be potentially explosive, so it is important to handle 1-Naphthalenamine, 8-azidowith care and follow proper safety precautions to minimize the risk of accidents.
Check Digit Verification of cas no
The CAS Registry Mumber 2112-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2112-98:
(6*2)+(5*1)+(4*1)+(3*2)+(2*9)+(1*8)=53
53 % 10 = 3
So 2112-98-3 is a valid CAS Registry Number.