Ordering
Available Variants1 g
CHA.18613-1g
Price
€42.64
Available – Dispatch in 14 days
5 g
CHA.18613-5g
Price
€171.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.18613-1g | €42.64 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.18613-5g | €171.20 |
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) | C7H7Br2N |
|---|---|
| CAS Number | 7703-74-4 |
| Molecular Weight | 264.95 |
| NACRES | NA.22 |
| PubChem Substance ID | 24865316 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00191795 |
| Assay | 98% |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302,H315,H319,H335 |
| pcodes | P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - 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, Gloves |
Technical Overview & Applications Use-case context
2,6-Bis(bromomethyl)pyridine, with the CAS registry number 7703-74-4, is a chemical compound that has garnered significant attention in the realm of organic chemistry. This pyridine derivative is characterized by the presence of two bromomethyl groups attached to the 2 and 6 positions of the pyridine ring, rendering it a versatile intermediate in various synthetic transformations. The compounds unique structure allows it to participate in a range of reactions, including nucleophilic substitution and cross-coupling reactions, making it a valuable building block in the synthesis of complex molecules. As a result, 2,6-Bis(bromomethyl)pyridine has found applications in the preparation of pharmaceuticals, agrochemicals, and materials science, highlighting its importance in modern chemical research and development. Its reactivity and accessibility have made it a sought-after compound in many laboratories worldwide.
