Discover the magic of the 4-Nitrophenylethylamine hydrochloride

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 29968-78-3. Application In Synthesis of 4-Nitrophenylethylamine hydrochloride.

Research speed reading in 2021. The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 29968-78-3, Name is 4-Nitrophenylethylamine hydrochloride, molecular formula is C8H11ClN2O2. In an article, author is Dong, YK,once mentioned of 29968-78-3, Application In Synthesis of 4-Nitrophenylethylamine hydrochloride.

Mirror symmetry in 7,9-dibenzyl-1-tert-butoxycarbonyl-1,7,9-triazaspiro[4.5]dec-3-en-2-one

The crystal structure of tert-butyl 7,9-dibenzyl-2-oxo-1,7,9-triazaspiro[4.5]dec-3-ene-1-carboxylate, C26H31N3O3, is reported. The molecule has imposed mirror symmetry and the hexahydropyrimidine ring adopts a chair conformation with two benzyl substituents bonded equatorially to the ring N atoms. The 3-pyrrolin-2-one is attached as a spiro-skeleton to the hexahydropyrimidine ring by one axial C-C and one equatorial C-N bond.

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 29968-78-3. Application In Synthesis of 4-Nitrophenylethylamine hydrochloride.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem