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- CAS号：
284462-37-9
[4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide
284462-37-9
C₁₃H₁₃N₃O₂
243.26
Light Brown to Brown Solid
DMSO (Slightly), Methanol (Slightly)
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文献和实验[4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide
284462-37-9
C₁₃H₁₃N₃O₂
243.26
Light Brown to Brown Solid
DMSO (Slightly), Methanol (Slightly)
General Laboratory Methods for Tetrapyrroles
-pyrrole positions, at the four meso [5,10,15,20] carbon atoms, and N-alkyl groups can be added to the four central nitrogen atoms. Since its synthesis in 1972, over 8000 literature references have appeared on 5,10,15, 20-tetrakis(N-methyl-4-pyridyl
Conjugation of 5′‐Functionalized Oligodeoxyribonucleotides with Properly Functionalized Ligands
‐Aminoalkylated Oligodeoxyribonucleotides to Ligands Functionalized with an Isothiocyanate or N‐Hydroxysuccinimidyl Group Basic Protocol 3: Conjugation of Oligodeoxyribonucleotide 5′‐Phosphorothioates to Ligands Functionalized
. Cieślak, J. and Beaucage, S.L. 2003. Thermolytic properties of 3‐(2‐pyridyl)‐1‐propyl and 2‐[N‐methyl‐N‐(2‐pyridyl)]aminoethyl phosphate/thiophosphate protecting groups in solid‐phase synthesis
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