83734-36-5

Basic information

• Product Name: 1,3,5-tris(2-chlorophenyl)-1,3,5-triazinane
• CAS NO: 83734-36-5
• Molecular Formula: C₂₁H₁₈Cl₃N₃
• Molecular Weight: 418.7467
• Mol File: 83734-36-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 563.7°C at 760 mmHg
• Flash Point: 294.7°C
• Density: 1.359g/cm³
• Vapor Pressure: 9.9E-13mmHg at 25°C
• Refractive Index: 1.651
• CAS DataBase Reference: 1,3,5-tris(2-chlorophenyl)-1,3,5-triazinane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tris(2-chlorophenyl)-1,3,5-triazinane(83734-36-5)
• EPA Substance Registry System: 1,3,5-tris(2-chlorophenyl)-1,3,5-triazinane(83734-36-5)

Safety Data

• Hazardous Substances Data: 83734-36-5(Hazardous Substances Data)

Usage

Appearance

White crystalline solid

Uses

Intermediate in the synthesis of organic compounds
Herbicides
Pesticides
Dyes
Pharmaceuticals

Reactivity

Highly reactive

Reactions

Can undergo substitution reactions with nucleophiles (e.g., amines and alcohols)

Derivative compounds

Forms a wide range of derivative compounds

Polymer and resin production

Used in the production of cross-linked polymers and resins

Water treatment

Acts as a chlorine donor in water treatment applications

Health and environmental hazards

Poses significant health and environmental risks

Exposure management

Exposure to the compound should be carefully managed and controlled

Upstream product

• 50-00-0 formaldehyd 
• 64-17-5 ethanol 
• 95-51-2 o-chloroaniline 
• 352018-71-4 cycloheptane-1,1-diyl bis-hydroperoxide 

Relevant articles and documents

Synthesis of Diversely Substituted Imidazolidines via [3+2] Cycloaddition of 1,3,5-Triazinanes with Donor-Acceptor Aziridines and Their Anti-Tumor Activity

A Y(OTf)3-catalyzed [3+2] cycloaddition of 1,3,5-triazinanes with donor-acceptor aziridines has been developed, accessing diversely substituted imidazolidines high efficiency. Mechanistic investigations support the formation of imidazolidines through an SN1-like pathway. Furthermore, these imidazolidines exhibit promising anti-tumor activity against a series of human cancer cell lines. (Figure presented.).

Sm-Catalyzed Synthesis and Biological Activity of Acyclic and Cyclic Azadiperoxides

Acyclic diaminodiperoxides and cyclic azadiperoxides are synthesized by the reaction of 1,1-bis-(hydroperoxy)cycloalkanes with formaldehyde and primary arylamines in the presence of Sm-containing catalysts [SmCl3·6H2O, Sm(NO3/s

Synthesis of N-substituted 1,3,5-triazacyclohexanes catalyzed by starch sulfuric acid

N-substituted 1,3,5-triazacyclohexanes were simply synthesized from the reaction of aromatic or fatty amines and formaldehyde catalyzed by recyclable starch sulfuric acid with good yields at room temperature.