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Specifications
| Appearance | Light yellow powder |
| Purity(HPLC) | 99.5% min |
| MP | 216.0~220.0℃ |
Applications
1. Pharmaceutical Research
CBZO is a key intermediate in the synthesis of antiviral, anticancer, and anti-inflammatory drug candidates.
Triazole-containing compounds like CBZO are bioisosteres of amides and other pharmacophores, making them valuable for modifying drug-like properties.
2. Medicinal Chemistry Scaffold
The 1,2,3-triazole moiety is well known for its metabolic stability, hydrogen bonding capabilities, and bioactivity enhancement.
CBZO is often used in the design of kinase inhibitors, enzyme blockers, and protein–protein interaction disruptors.
3. Chemical Synthesis Intermediate
Acts as a building block in the synthesis of heterocyclic compounds, particularly those targeting pathogenic organisms or cancer cells.
Useful in click chemistry, particularly CuAAC (Copper(I)-catalyzed Azide-Alkyne Cycloaddition) strategies for rapid library synthesis.
4. Agrochemical Research
Triazole-containing carboxylic acids like CBZO may serve as lead structures or intermediates in the development of fungicides or plant growth regulators.
Benefits
✅ Biologically Privileged Structure
The triazole ring is recognized for its broad-spectrum bioactivity, low toxicity, and excellent pharmacokinetics.
✅ Chemical Stability
CBZO is chemically robust under a wide range of conditions, allowing it to be used in multi-step synthesis.
✅ Versatile Reactivity
The carboxylic acid group enables easy conjugation, amide bond formation, or esterification, making CBZO suitable for chemical diversification.
✅ Facilitates Medicinal Optimization
As a functionalized triazole, CBZO provides sites for SAR (Structure-Activity Relationship) studies, enhancing drug candidate fine-tuning.
Conclusion
CBZO (CAS 1199616-66-4) is a valuable synthetic intermediate and medicinal chemistry scaffold, featuring a 1,2,3-triazole core and a carboxylic acid group, making it ideal for drug development, lead compound optimization, and bioactive molecule design. Its versatility, bioisosteric value, and compatibility with modern synthetic techniques-especially click chemistry-position it as an important molecule in pharmaceutical R&D and chemical biology.
