13199-80-9 Usage
Description
2-(PYRIDIN-3-YLAMINOMETHYL)-PHENOL, a chemical compound with the molecular formula C12H11N2O, is a phenol derivative featuring a pyridine ring attached to the third carbon atom. 2-(PYRIDIN-3-YLAMINOMETHYL)-PHENOL has garnered interest due to its potential biological activities, such as anti-diabetic and anti-inflammatory properties. It serves as a valuable building block in organic chemistry and holds promise for applications in drug development and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
2-(PYRIDIN-3-YLAMINOMETHYL)-PHENOL is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals for its potential biological activities. Its anti-diabetic and anti-inflammatory properties make it a promising candidate for the development of new drugs targeting these conditions.
Used in Organic Chemistry:
2-(PYRIDIN-3-YLAMINOMETHYL)-PHENOL is used as a versatile building block in organic chemistry for its ability to form a wide range of chemical structures. Its unique combination of functional groups allows for various synthetic transformations, making it a valuable component in the creation of complex organic molecules.
Used in Medicinal Chemistry:
2-(PYRIDIN-3-YLAMINOMETHYL)-PHENOL is used as a starting material in medicinal chemistry for the design and synthesis of novel therapeutic agents. Its potential biological activities, such as anti-diabetic and anti-inflammatory effects, provide a foundation for the development of new drugs to treat various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 13199-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,9 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13199-80:
(7*1)+(6*3)+(5*1)+(4*9)+(3*9)+(2*8)+(1*0)=109
109 % 10 = 9
So 13199-80-9 is a valid CAS Registry Number.
13199-80-9Relevant articles and documents
Synthesis and biological activity of some 3-aryl-3,4-dihydro-2h-benz[e]-1, 3-oxazines/6-bromo-3-aryl-3,4-dihydro-2h-benz[e]-1,3-oxazines
Shukla, Davender Kumar,Rani, Manju,Khan, Arif Ali,Tiwari, Kavita,Gupta, Rajinder K.
, p. 5921 - 5924 (2013/07/26)
N-(2-Hydroxy)-benzyl-arylamine (1) gives substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines/6-bromo-3-aryl-3,4-dihydro-2H-benz[e] -1,3-oxazines (2) on cyclization with formaldehyde in methanol within 0.5-1.0 h at 65-68 C in excellent yields. Th
