![4,6-Dichloropyrazolo[1,5-a]pyrazine molecular structure](/images/molecules/4-6-dichloropyrazolo-1-5-a-pyrazine-2127110-20-5.png)
Ordering
Available Variants500 mg
CHA.19063-500mg
Price
€198.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.19063-500mg | €198.40 |
≥95%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C6H3Cl2N3 |
|---|---|
| CAS Number | 2127110-20-5 |
| Molecular Weight | 188.01 |
| MDL number | MFCD31729103 |
| NACRES | NA.22 |
| Assay | ≥95% |
| Form | powder or crystals |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
4,6-Dichloropyrazolo[1,5-a]pyrazine, with the CAS registry number 2127110-20-5, is a synthetic organic compound belonging to the pyrazolo[1,5-a]pyrazine class. This compound exhibits a unique molecular structure, consisting of a fused ring system with two chlorine substituents at positions 4 and 6. The presence of these chlorine atoms imparts specific chemical and physical properties to the molecule, influencing its reactivity and potential applications. As a building block in organic synthesis, 4,6-Dichloropyrazolo[1,5-a]pyrazine can undergo various chemical transformations, such as nucleophilic substitution reactions, to yield a range of derivatives with diverse functional properties. Further research is needed to fully explore the potential of this compound and its derivatives in various fields, including pharmaceuticals, materials science, and agrochemistry. Its properties and reactivity make it an interesting subject for ongoing scientific investigation.
