1000981-41-8 Usage
Description
2-(6-Fluoro-pyridin-2-ylaMino)-ethanol is an organic compound characterized by the presence of a fluorine atom on the pyridine ring and an amino group attached to the ethyl moiety. This unique structure endows it with specific chemical properties that make it a valuable intermediate in the synthesis of various pharmaceuticals and organic compounds.
Uses
Used in Pharmaceutical Industry:
2-(6-Fluoro-pyridin-2-ylaMino)-ethanol is used as a key reactant for the preparation of substituted bicyclic pyridones, which are important structural motifs in the development of novel pharmaceutical agents. These bicyclic pyridones exhibit a range of biological activities, including antimicrobial, antiviral, and anticancer properties, making them valuable for the treatment of various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(6-Fluoro-pyridin-2-ylaMino)-ethanol serves as a versatile building block for the synthesis of a wide array of organic compounds. Its unique structure allows for various chemical transformations, such as nucleophilic substitution, electrophilic aromatic substitution, and reductive amination, enabling the creation of diverse molecular architectures with potential applications in materials science, agrochemicals, and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1000981-41-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,9,8 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1000981-41:
(9*1)+(8*0)+(7*0)+(6*0)+(5*9)+(4*8)+(3*1)+(2*4)+(1*1)=98
98 % 10 = 8
So 1000981-41-8 is a valid CAS Registry Number.
1000981-41-8Relevant articles and documents
COLOUR AND CONSTITUTION OF AZO COMPOUNDS DERIVED FROM DIAMINOAZINES
Hutchings, Michael G.,Meyrick, Barry H.,Nelson, Anthony J.
, p. 5081 - 5088 (1984)
Visible absorption spectra have been recorded for azo compounds derived from 2,5-dichlorosulphanilic acid azo-coupled with N,N-diethyl-m-phenylenediamine, and with azine analogues.The effects of the ring-aza substituents as well as cyano on the spectra indicate a surprising difference in sensitivity of the two ring positions meta to the azo group.M.O. calculations show that the amino group ortho to the azo linkage introduces asymmetry into the HOMO, and this is responsible for the differing effects of substitution.
