24015-99-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Pyridinamine,3-(2-propenyloxy)-(9CI) is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and chemical properties allow it to be a versatile building block for the development of new drugs.
Used in Organic Synthesis:
2-Pyridinamine,3-(2-propenyloxy)-(9CI) is used as a reagent in organic synthesis for the preparation of various organic compounds. Its pyridine ring and propenyl group provide opportunities for further chemical reactions and modifications.
It is important to handle and use 2-Pyridinamine,3-(2-propenyloxy)-(9CI) with caution, following proper safety protocols and regulations, due to its potential hazards and risks associated with its handling and exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 24015-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,1 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24015-99:
(7*2)+(6*4)+(5*0)+(4*1)+(3*5)+(2*9)+(1*9)=84
84 % 10 = 4
So 24015-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O/c1-2-6-11-7-4-3-5-10-8(7)9/h2-5H,1,6H2,(H2,9,10)
24015-99-4Relevant academic research and scientific papers
Ligandless copper-catalyzed coupling of heteroaryl bromides with gaseous ammonia
Fantasia, Serena,Windisch, Johannes,Scalone, Michelangelo
, p. 627 - 631 (2013/04/11)
A range of different N- and S-containing heterocyclic bromides can be efficiently coupled with gaseous ammonia in the presence of copper(II) acetylacetonate [Cu(acac)2] as catalyst and in the absence of additional ligands. Unstable aminothiophenes and aminobenzothiophenes can be further reacted in situ to afford functionalized derivatives. Copyright
SYNTHESIS OF NEW HETEROCYCLIC PHENOLS: 8-HYDROXY-IMIDAZOPYRIDINE
Rydzkowski, R.,Blondeau, D.,Sliwa, H.
, p. 2571 - 2574 (2007/10/02)
Preparation of the unknown title compound has been achieved by condensation of 2-amino-3-hydroxy-pyridine with chloroacetaldehyde.Activation by the free phenolic hydroxyl allows preferential nitration of the pyridine ring, in marked contrast to the behavior of the related ethers which suffer electrophilic substitution on the imidazole moiety, as usual in the series.
