128798-29-8

Basic information

• Product Name: N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE
• Synonyms: N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE;N-(4-PHENYLCYCLOHEXENYL)FORMAMIDE
• CAS NO: 128798-29-8
• Molecular Formula: C₁₃H₁₅NO
• Molecular Weight: 201.26
• Mol File: 128798-29-8.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE(128798-29-8)
• EPA Substance Registry System: N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE(128798-29-8)

Safety Data

• Hazardous Substances Data: 128798-29-8(Hazardous Substances Data)

Usage

General Description

N-(4-phenyl-cyclohex-1-enyl)-formamide is an organic compound with the molecular formula C13H13NO. It is a formamide derivative with a cyclohexene ring substituted with a phenyl group at the 4-position. N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential antitumor and antibacterial properties. N-(4-phenyl-cyclohex-1-enyl)-formamide is a white solid that is soluble in organic solvents and has a melting point of 98-102°C. It is important to handle this compound with caution as it may cause skin and eye irritation.

Upstream product

• 4894-75-1 1-phenyl-4-cyclohexanone 
• 77287-34-4 formamide 
• 128828-07-9 C₁₉H₂₁NS 
• 2258-42-6 formyl acetic anhydride 

Downstream Products

• 128798-39-0 rac-4-phenyl-cyclohexen-1-yl-isocyanide 
• 128798-35-6 1-Isocyano-4-phenyl-7-oxa-bicyclo[4.1.0]heptane 
• 292072-85-6 rac-1-[(2-benzyloxycarbonyl-aminoethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-phenyl-cyclohexen-1-yl)-amide 
• 255736-19-7 rac-1-[(2-tert-butyloxycarbonyl-aminoethyl)-thyminacetyl-amino]-cyclohexancarboxylic acid-(4-phenyl-cyclohexen-1-yl)-amide 

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.