46425-73-4

Basic information

• Product Name: N-(2-Chlorobenzyl)cyclohexanamine
• Synonyms: N-(2-Chlorobenzyl)cyclohexanamine
• CAS NO: 46425-73-4
• Molecular Formula: C₁₃H₁₈ClN
• Molecular Weight: 223.74172
• Mol File: 46425-73-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 167-169 °C(Press: 12 Torr)
• Appearance: /
• Density: 1.08±0.1 g/cm3(Predicted)
• PKA: 9.31±0.20(Predicted)
• CAS DataBase Reference: N-(2-Chlorobenzyl)cyclohexanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Chlorobenzyl)cyclohexanamine(46425-73-4)
• EPA Substance Registry System: N-(2-Chlorobenzyl)cyclohexanamine(46425-73-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 46425-73-4(Hazardous Substances Data)

Upstream product

• 108-91-8 cyclohexylamine 
• 89-98-5 2-chloro-benzaldehyde 
• 115765-22-5 N-(2-chlorobenzylidene)cyclohexylamine 

Relevant articles and documents

Design, Synthesis, and Structure-Activity Relationship of Economical Triazole Sulfonamide Aryl Derivatives with High Fungicidal Activity

Plant fungal diseases have caused great decreases in crop quality and yield. As one of the considerable agricultural diseases, cucumber downy mildew (CDM) caused by pseudoperonospora cubensis seriously influences the production of cucumber. Amisulbrom is a commercial agricultural fungicide developed by Nissan Chemical, Ltd., for the control of oomycetes diseases that is highly effective against CDM. However, the synthesis of amisulbrom has a high cost because of the introduction of the bromoindole ring. In addition, the continuous use of amisulbrom might increase the risk of resistance development. Hence, there is an imperative to develop active fungicides with new scaffolds but low cost against CDM. In this study, a series of 1,2,4-triazole-1,3-disulfonamide derivatives were designed, synthesized, and screened. Compound 1j showed a comparable fungicidal activity with amisulbrom, but it was low cost and ecofriendly. It has the potential to be developed as a new fungicide candidate against CDM. Further investigations of structure-activity relationship exhibited the structural requirements of 1,2,4-triazole-1,3-disulfonamide and appropriate modification in N-alkyl benzylamine groups with high fungicidal activity. This research will provide powerful guidance for the design of highly active lead compounds with a novel skeleton and low cost.

Catalytic Asymmetric Synthesis of N-Chiral Amine Oxides

Direct asymmetric synthesis of N-chiral amine oxides was accomplished (up to 91:9 e.r.) by means of a bimetallic titanium catalyst. A hydroxy group situated at the γ-position of the N stereocenter enables the desired N-oxidation through dynamic kinetic resolution of the trivalent amine substrates. The method was further extended to the kinetic resolution of racemic γ-amino alcohols with a preexisting stereocenter, giving an important class of enantioenriched (up to 99.9:0.1 e.r.) building blocks that are otherwise difficult to synthesize.

A new method for the reduction of amides with zinc ethanol

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