2,4-Dichloro-6-phenyl-1,3,5-triazine丨CAS 1700-02-3

2,4-Dichloro-6-phenyl-1,3,5-triazine丨CAS 1700-02-3
Product Introduction:
Catalog No.: SS083102
CAS No.: 1700-02-3
Purity(GC): 99.0% min
Product Name: 2,4-Dichloro-6-phenyl-1,3,5-triazine
Molecular Formula: C9H5Cl2N3
Molecular Weight: 226.06
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Technical Parameters
Description

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Specifications of 2,4-Dichloro-6-phenyl-1,3,5-triazine丨CAS 1700-02-3

 

Appearance

Off-white or light-yellow solid

Purity (GC)

99.0% min

Melting Point

116.0~122.0℃

 

 

 

Chemical Overview

2,4-Dichloro-6-phenyl-1,3,5-triazine丨CAS 1700-02-3 belongs to the class of s-triazine derivatives, characterized by a six-membered aromatic ring containing three nitrogen atoms at alternating positions. The two chlorine atoms and one phenyl substituent at the 2, 4, and 6 positions, respectively, make it a highly reactive intermediate for chemical synthesis.


 

Applications of 2,4-Dichloro-6-phenyl-1,3,5-triazine

1. Intermediate in Herbicide and Pesticide Synthesis

It is a key intermediate in the manufacture of triazine-based herbicides, such as atrazine and simazine.

Used in the production of agrochemical compounds with broad-spectrum weed control properties.

Its reactive chlorine atoms enable nucleophilic substitution reactions to modify the molecule and tailor herbicidal activity.

2. Building Block for Dyes and Fluorescent Compounds

2,4-Dichloro-6-phenyl-1,3,5-triazine丨CAS 1700-02-3 serves as a precursor in the synthesis of reactive dyes for textiles.

Triazine moiety imparts thermal and chemical stability to dyes.

Used in the creation of fluorescent probes and sensors for biochemical applications.

3. Pharmaceutical Synthesis Intermediate

Applied in the design and synthesis of heterocyclic pharmaceutical compounds.

Its triazine ring system is a common scaffold in medicinal chemistry for developing antiviral, anticancer, and antimicrobial agents.

Enables functionalization via chlorine substitution to introduce diverse pharmacophores.

4. Polymer and Resin Chemistry

Used as a crosslinking agent or curing agent for epoxy and phenolic resins.

Enhances thermal stability, chemical resistance, and mechanical strength of polymer materials.

Serves in the production of specialty polymers for coatings, adhesives, and composites.

5. Photographic and Imaging Chemicals

Employed in photographic chemistry as a reagent or intermediate.

Utilized in the synthesis of photosensitive compounds and photoresists in microfabrication and electronics.


 

Benefits of 2,4-Dichloro-6-phenyl-1,3,5-triazine

1. High Chemical Reactivity

The chlorine atoms at the 2 and 4 positions are highly reactive, allowing easy substitution by various nucleophiles.

This facilitates the creation of a wide variety of derivatives for tailored applications.

2. Versatility

Serves as a multifunctional building block across multiple industries-agrochemical, pharmaceutical, dye, and polymer industries.

Enables rapid development of new compounds through straightforward synthetic routes.

3. Thermal and Chemical Stability

The triazine ring imparts high thermal stability and resistance to hydrolysis and oxidation.

Makes derivatives suitable for harsh processing conditions in polymer and dye manufacturing.

4. Enhances Product Performance

Products derived from this compound (e.g., herbicides, dyes, polymers) often show improved efficacy, durability, and environmental tolerance.

Crosslinked polymers formed with triazine agents demonstrate superior mechanical strength and chemical resistance.

5. Cost-Effective Intermediate

Compared to more complex heterocyclic intermediates, this compound is relatively inexpensive and readily available.

Its efficient reactivity reduces the number of synthetic steps required, saving time and resources.

6. Supports Sustainable Agriculture

Use in herbicide synthesis helps promote effective weed control and crop yield improvement.

Allows for the design of herbicides with targeted action, potentially reducing environmental impact.


 

Conclusion

2,4-Dichloro-6-phenyl-1,3,5-triazine丨CAS 1700-02-3 is a pivotal chemical intermediate with extensive applications in agrochemical synthesis, pharmaceutical development, dye manufacturing, and polymer chemistry. Its reactive dichlorotriazine core provides a versatile platform for chemical modifications, enabling the creation of high-performance products. The combination of chemical stability, reactivity, and cost-effectiveness makes it a valuable compound in both industrial and research settings, especially in the production of herbicides and specialty materials.

 

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