128798-29-8 Usage
Uses
Used in Pharmaceutical Industry:
N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE is used as an intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE serves as an intermediate, playing a role in the creation of compounds used in agricultural chemicals.
Used in Antitumor Research:
N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE is used as a subject of study in antitumor research due to its potential antitumor properties, which could lead to advancements in cancer treatment.
Used in Antibacterial Applications:
N-(4-PHENYL-CYCLOHEX-1-ENYL)-FORMAMIDE is also utilized in antibacterial research, exploring its potential to combat bacterial infections, given its noted antibacterial properties.
Check Digit Verification of cas no
The CAS Registry Mumber 128798-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,9 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 128798-29:
(8*1)+(7*2)+(6*8)+(5*7)+(4*9)+(3*8)+(2*2)+(1*9)=178
178 % 10 = 8
So 128798-29-8 is a valid CAS Registry Number.
128798-29-8Relevant academic research and scientific papers
Multicomponent synthesis of novel amino acid-nucleobase chimeras: aA versatile approach to PNA-monomers
Maison, Wolfgang,Schlemminger, Imre,Westerhoff, Ole,Martens, Juergen
, p. 1343 - 1360 (2007/10/03)
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.
A New And Mild Procedure For The Preparation Of Vinyl Formamides From Thiooximes
Baldwin, J.E.,Aldous, D.J.,ONeil, I.A.
, p. 2051 - 2054 (2007/10/02)
Treatment of thiooximes with triphenylphosphine and acetic formic anhydride in dichloromethane at room temperature gives good yields of vinyl formamides under essentially neutral conditions.
