32997-99-2

Basic information

• Product Name: 6-Chloro-N(2),N(4)-dicyclohexyl-1,3,5-triazine-2,4-diamine
• CAS NO: 32997-99-2
• Molecular Formula: C₁₅H₂₄ClN₅
• Molecular Weight: 309.842
• Mol File: 32997-99-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-Chloro-N(2),N(4)-dicyclohexyl-1,3,5-triazine-2,4-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Chloro-N(2),N(4)-dicyclohexyl-1,3,5-triazine-2,4-diamine(32997-99-2)
• EPA Substance Registry System: 6-Chloro-N(2),N(4)-dicyclohexyl-1,3,5-triazine-2,4-diamine(32997-99-2)

Safety Data

• Hazardous Substances Data: 32997-99-2(Hazardous Substances Data)

Usage

Type

Synthetic organic compound

Function

Insect growth regulator and pesticide

Mode of Action

Inhibits the development of larvae into adult insects

Effective Against

Flies, maggots, beetles

Use

Agricultural and veterinary settings

Target Pests

Insects resistant to other pesticides

Caution

Harmful to non-target insects and aquatic organisms.

Upstream product

• 108-91-8 cyclohexylamine 
• 27282-86-6 6-cyclohexylamino-2,4-dichloro-1,3,5-triazine 

Downstream Products

• 1363418-54-5 N⁽²⁾,N⁽⁴⁾-dicyclohexyl-6-(piperazin-1-yl)-1,3,5-triazine-2,4-diamine 
• 43167-87-9 N,N'-dicyclohexyl-6-morpholin-4-yl-[1,3,5]triazine-2,4-diamine 

Relevant articles and documents

Design, facile synthesis, antibacterial activity and structure-activity relationship of novel di- and tri-substituted 1,3,5-triazines

Due to overwhelming generation of drug resistant microorganisms, there is an urgent need to develop novel chemotherapeutic agents. In continuation of our research on discovery of novel heterocyclic scaffolds from 1,3,5-triazine, present study deals with design and development of some novel di- and tri-substituted 1,3,5-triazine derivatives. The synthesis of title analogues were accomplished by SNAr reaction and subsequently underwent rigorous antibacterial screening against a panel of representative Gram-negative and Gram-positive bacteria. Screening results revealed that minor structural variation may induce drastic changes in activity. Whereas, amine bridge and piprazine was termed as pivotal structural fragments necessary for generation and escalation of bio-activity. The structures of newly synthesized compounds were ascertained on the basis of their analytical and spectral profiles.