CAS 3703-10-4

4,6-dichloro-N-(propan-2-yl)-1,3,5-triazin-2-amine

Description:

4,6-Dichloro-N-(propan-2-yl)-1,3,5-triazin-2-amine, commonly known as a herbicide, belongs to the triazine class of compounds. It features a triazine ring, which is a six-membered aromatic heterocycle containing three nitrogen atoms. This compound is characterized by the presence of two chlorine atoms at the 4 and 6 positions of the triazine ring, which enhances its herbicidal activity. The N-(propan-2-yl) substituent indicates that there is an isopropyl group attached to the nitrogen atom, contributing to its lipophilicity and potential for bioactivity. The compound is typically used in agricultural applications for weed control, acting by inhibiting photosynthesis in target plants. Its stability and solubility in various solvents make it effective in formulations. However, like many triazines, it may pose environmental concerns, particularly regarding water contamination and effects on non-target organisms. Proper handling and application are essential to mitigate risks associated with its use.

Formula: C₆H₈Cl₂N₄

InChI: InChI=1/C6H8Cl2N4/c1-3(2)9-6-11-4(7)10-5(8)12-6/h3H,1-2H3,(H,9,10,11,12)

SMILES: CC(C)N=c1[nH]c(Cl)nc(Cl)n1

Synonyms:

• 1,3,5-Triazin-2-amine, 4,6-dichloro-N-(1-methylethyl)-

2,4-Dichloro-6-isopropylamino-1,3,5-triazine

Controlled Product

CAS: 3703-10-4

Applications 2,4-Dichloro-6-isopropylamino-1,3,5-triazine is an intermediate in the synthesis of Atrazine-d5 (A794602). Atrazine-d5 is a labelled selective herbicide. Potential symptoms of overexposure are irritation of eyes and skin; dermatitis, skin sensitization; dyspnea, weakness, incoordination, salivation; hypothermia and liver injury.
References Dalgaard-Mikkelsen, S., et al.: Pharmacol. Rev., 14, 225 (1962); Muller, K., et al.: J. Environ. Qual., 31, 309 (2002); Backhaus, T., et al.: Environ. Toxicol. Chem., 23, 258 (2004)

Formula: C₇H₉FN₂O₂S

Color and Shape: Neat

Molecular weight: 204.222

Ref: TR-D438405