2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6

2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6
Product Introduction:
Catalog No.: SS118285
CAS No.: 3140-73-6
Purity: 99.0%min
Product Name: 2-Chloro-4,6-dimethoxy-1,3,5-triazine
Molecular Formula: C5H6ClN3O2
Molecular Weight: 175.57
Send Inquiry
Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 2-chloro-4,6-dimethoxy-1,3,5-triazine丨cas 3140-73-6 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications of 2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6

 

Appearance:

White crystalline powder

Purity:

99.0% min

Melting point:

71~78℃

Moisture:

0.1% max

 

 

Transport Information of 2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6

 

Parameter

Specification

UN Number

3077

Class

 

Packing Group

 

H.S. Code

2933699099999

Stability & Reactivity

The product is chemically stable under standard ambient conditions (room temperature).

Storage

Inert atmosphere, Room Temperature

Condition to Avoid

 

Package

 

 

Manufacturing Information of 2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6

 

Parameter

Specification

Capacity

500kg/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

 

Stock

 

2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6 (CDMT) is a highly versatile reagent used in organic synthesis, particularly for peptide coupling and activation of carboxylic acids. As a derivative of triazine, it offers selective reactivity and mild activation properties, making it valuable in pharmaceutical, biochemical, and materials science applications.

 

Key Applications of 2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6

 

1. Peptide Synthesis
● CDMT is widely used as a coupling reagent for peptide bond formation.
● It facilitates the conversion of carboxylic acids to activated esters, which then react with amines to form amide bonds.
● Preferred for solid-phase peptide synthesis (SPPS) due to its mild reaction conditions and high yields.
2. Activation of Carboxylic Acids
● CDMT is employed to activate carboxylic acids into reactive intermediates, such as triazine esters, that readily undergo nucleophilic substitution.
● Useful in forming esters, amides, and lactones in complex organic synthesis.
3. Pharmaceutical and Biochemical Applications
● Utilized in the synthesis of drug intermediates, bioactive molecules, and protein conjugates.
● Enables selective modification of biomolecules without harsh reagents or high temperatures.
4. Polymer and Materials Chemistry
● Acts as a crosslinking agent or functionalizing group in polymers containing carboxyl or amino functionalities.
● Enhances compatibility and reactivity in coatings, adhesives, and functional materials.

 

Benefits of 2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6

 

✅ High Reactivity with Carboxylic Acids
● 2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6 provides efficient activation under mild conditions, avoiding racemization-a crucial factor in chiral synthesis.
✅ Mild and Clean Reactions
● Does not generate toxic byproducts; easy to remove residual materials post-reaction.
● Compatible with a wide range of solvents and functional groups.
✅ Enhanced Selectivity
● Offers better selectivity compared to traditional reagents (e.g., DCC or EDC) in forming amide bonds or acylated compounds.
✅ Useful in Aqueous or Organic Media
● CDMT-based reactions can be conducted in both aqueous and organic solvents, offering versatility in lab-scale and industrial processes.
✅ Improves Yield and Efficiency
● Often leads to higher coupling efficiency, reducing the need for excess reagents or repeated purification steps.

 

Conclusion

 

2-Chloro-4,6-dimethoxy-1,3,5-triazine丨CAS 3140-73-6 is a powerful and selective activation reagent ideal for amide and ester synthesis, especially in peptide chemistry. Its efficient reactivity, mild conditions, and clean conversion pathways make it a go-to choice for synthetic chemists working in drug development, materials science, and bioconjugation.

 

Send Inquiry
Beyond Your Expectation
From Science to Life with LEAPChem
contact us