292072-97-0

Basic information

• Product Name: rac-2-[(2-benzyloxyethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-tert-butyl-cyclohexen-1-yl)-amide
• Synonyms: rac-2-[(2-benzyloxyethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-tert-butyl-cyclohexen-1-yl)-amide
• CAS NO: 292072-97-0
• Molecular Weight: 578.752
• Mol File: 292072-97-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: rac-2-[(2-benzyloxyethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-tert-butyl-cyclohexen-1-yl)-amide(CAS DataBase Reference)
• NIST Chemistry Reference: rac-2-[(2-benzyloxyethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-tert-butyl-cyclohexen-1-yl)-amide(292072-97-0)
• EPA Substance Registry System: rac-2-[(2-benzyloxyethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-tert-butyl-cyclohexen-1-yl)-amide(292072-97-0)

Safety Data

• Hazardous Substances Data: 292072-97-0(Hazardous Substances Data)

Upstream product

• 98-53-3 4-tercbutyl-cyclohexanone 
• 255735-91-2 rac-N-4-tert-butyl-cyclohex-1-enyl-formamide 
• 20924-05-4 thymidyl acetic acid 
• 38336-04-8 O-benzylethanolamine 
• 108-94-1 cyclohexanone 
• 223252-57-1 rac-4-tert-butyl-cyclohexen-1-yl-isocyanide 

Relevant articles and documents

Multicomponent synthesis of novel amino acid-nucleobase chimeras: aA versatile approach to PNA-monomers

This paper describes a multicomponent approach to novel totally protected precursors of PNA-monomers via Ugi 4CC. The obtained bisamides are converted into several partially protected PNA-monomers or derivatives thereof using three different procedures. Methods for hydrolysis are shown to be dependent on the nature of the isocyano component required for Ugi 4CC. Several novel monomers suitable for oligomer synthesis are prepared demonstrating the high versatility of the reaction sequence. Copyright (C) 2000 Elsevier Science Ltd.