Ordering
Available Variants5 g
CHA.75794-5g
Price
€21.20
Available – Dispatch in 14 days
25 g
CHA.75794-25g
Price
€79.12
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.75794-5g | €21.20 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.75794-25g | €79.12 |
98%
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) | C5H4Cl2N2 |
|---|---|
| CAS Number | 1780-26-3 |
| Molecular Weight | 163.00 |
| NACRES | NA.22 |
| PubChem Substance ID | 24881648 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00090472 |
| Assay | 98% |
Safety Information Handling visibility
| pictograms |
GHS07
GHS09
  GHS07,GHS09
|
|---|---|
| signalword | Warning |
| hcodes | H302,H317,H411 |
| pcodes | P273 - P280 - P301 + P312 + P330 - P302 + P352 |
| Hazard Classifications | Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | 208.0 °F - closed cup |
| flash_point_c | 97.78 °C - closed cup |
| ppe | Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
4,6-Dichloro-2-methylpyrimidine, with the CAS registry number 1780-26-3, is a synthetic organic compound belonging to the pyrimidine class. This chemical intermediate is utilized in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compounds structure consists of a pyrimidine ring with two chlorine atoms at positions 4 and 6, and a methyl group at position 2. Its reactivity is characterized by the presence of the two chlorine atoms, which can undergo nucleophilic substitution reactions, allowing for the introduction of other functional groups. As a result, 4,6-dichloro-2-methylpyrimidine serves as a versatile building block in the synthesis of complex molecules, and its applications continue to expand in fields such as medicine and agriculture, where the development of new compounds with specific properties is essential. Its properties and reactivity make it a valuable intermediate in various chemical syntheses.
