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N-(Dimethylethyl)-1,2,3,4-Tetrahydro-3-Isoquilolinecarboxamide
Category : Intermediates
CAS NO : 149182-72-9 EC NO : MF : C14H21N2O MW : 233.3288 Product description : Chemical name: (S)-N-tert-Butyl-1,2,3,4-tetrahydroisoquinoline-3-carboxamide CAS:149182-72-9 Molecular formula:C14H20N2O Molecular weight:232.32 Appearance: Content:99% Synonyms : [(3s)-(3-1,2,3,4-Tetrahydroisoquinolyl)]-N-(Tert-Butyl)Carboxamide;(3s)-N-(Tert-Butyl)-1,2,3,4-Tetrahydroisoquinoline-3-Carboxamide;(S)-(-)-N-Tert-Butyl-1,2,3,4-Tetrahydro-3-Isoquinolinecarboxamide;(S)-N-T-Butyl Tetrahydro-3-Iso-Quinoline-Carboxamide;(3s)-1,2,3,4-Tetrahydroisoquinoline-3-(N-Tert-Butylcarboxamide);(S)-(-)-N-Tert-Butyl-1,2,3,4-Tetrahydro-;(S)-N-Tert-Butyl-1,2,3,4-Tetrahydroisoquinoline-3-Carboxamide;(3s)-N-Tetrbutyl-1,2,3,4-Tetrahydroisoquinoline-3-Carboxamide;(3s)-(S-1,2,3,4-Tetrahydoisoquinolyl)]-N-(Tert-Butyl)Carboxamide;(3s)-N-Tert-Butyl-3,4-Dihydro-1h-Isoquinoline-3-Carboxamide;N-(Dimethylethyl)-1,2,3,4-Tetrahydro-3-Isoquilolinecarboxamide;(3S)-3-(tert-butylcarbamoyl)-1,2,3,4-tetrahydroisoquinolinium;N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3(s)-carboxamide; Molecular Structure : 
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- ? Friede-Crafts
- ? Acylation Reaction
- ? Grignard
- ? Alkali fusion
- ? Sulfonation
- ? Displacement Reaction
- ? Diazoniation
- ? Halogenation
- ? Chlorination
- ? Fluorination
- ? Bromination
- ? Reduction
- ? Nitration
- ? Easterification
- ? Alkylation
- ? 3-nitro-4-amino phenol
- ? 3-nitro-4-methyl phenol
- ? 2-methyl-5-amino phenol