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Available Variants1 g
CHA.33728-1g
Price
€40.68
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.33728-1g | €40.68 |
97%
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.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C5H2Cl2IN |
|---|---|
| CAS Number | 98027-84-0 |
| Molecular Weight | 273.89 |
| NACRES | NA.22 |
| PubChem Substance ID | 24884011 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD07368400 |
| Assay | 97% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302,H315,H317,H318,H335 |
| pcodes | P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
Technical Overview & Applications Use-case context
2,6-Dichloro-4-iodopyridine, with the CAS registry number 98027-84-0, is a halogenated pyridine derivative that has garnered significant attention in the realm of organic synthesis. This compound exhibits a unique combination of reactivity and selectivity, rendering it a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials science applications. The presence of the iodine substituent at the 4-position allows for facile cross-coupling reactions, while the dichloro substituents at the 2- and 6-positions provide additional sites for further functionalization. As a result, 2,6-dichloro-4-iodopyridine has become a versatile building block in the synthesis of complex molecules, enabling the creation of diverse chemical libraries and the exploration of novel chemical space. Its applications continue to expand, driven by ongoing research and development efforts in various fields.
