141075-07-2

Basic information

• Product Name: Formamide, N-(2-chloro-6-nitrophenyl)-
• CAS NO: 141075-07-2
• Molecular Formula: C7H5ClN2O3
• Molecular Weight: 200.581
• Mol File: 141075-07-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Formamide, N-(2-chloro-6-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Formamide, N-(2-chloro-6-nitrophenyl)-(141075-07-2)
• EPA Substance Registry System: Formamide, N-(2-chloro-6-nitrophenyl)-(141075-07-2)

Safety Data

• Hazardous Substances Data: 141075-07-2(Hazardous Substances Data)

Upstream product

• 64-18-6 formic acid 
• 769-11-9 2-chloro-6-nitroaniline 

Downstream Products

• 1360448-88-9 1-(benzo[d]thiazol-4-yl)-3-phenylurea 
• 1123-51-9 4-aminobenzothiazol 

Relevant articles and documents

Structure-activity relationships of N-phenyl-N′-benzothiazol-6-ylurea synthetic derivatives: Cytokinin-like activity and adventitious rooting enhancement

Some years ago we demonstrated the cytokinin-like activity of the synthetic N-phenyl-N′-benzothiazol-6-ylurea (PBU) and a relevant adventitious rooting adjuvant activity of symmetric urea derivatives devoid of any cytokinin- or auxin-like activity per se. Here we report the synthesis and the biological activity evaluation of nine symmetric or asymmetric ureas/thioureas, structurally related to PBU. None of them show cytokinin-like activity, while we demonstrate for the first time that PBU interacts with Arabidopsis cytokinin receptor CRE1/AHK4 in a heterologous bioassay system. Among the PBU derivatives, all the symmetric ureas/thioureas show an adventitious rooting adjuvant activity in various bioassays, confirming that this activity is strictly dependent on their chemical structure.