Ordering
Available Variants1 g
CHA.23550-1g
Price
€118.40
Available – Dispatch in 14 days
5 g
CHA.23550-5g
Price
€512.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.23550-1g | €118.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.23550-5g | €512.80 |
≥96.5% (GC)
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) | C10H8BrN |
|---|---|
| CAS Number | 5632-15-5 |
| Molecular Weight | 222.08 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 329764327 |
| MDL number | MFCD08062399 |
| Beilstein/REAXYS Number | 115410 |
| Assay | ≥96.5% (GC) |
| Form | powder |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302,H318 |
| pcodes | P280 - P301 + P312 + P330 - P305 + P351 + P338 + P310 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Dam. 1 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
2-(Bromomethyl)quinoline, with the CAS registry number 5632-15-5, is a chemical compound that has been utilized in various organic synthesis reactions. This quinoline derivative is characterized by the presence of a bromomethyl group attached to the second position of the quinoline ring, which renders it a versatile intermediate for further chemical transformations. The compounds reactivity is primarily attributed to the bromine atom, which can undergo nucleophilic substitution reactions, allowing for the introduction of diverse functional groups. As such, 2-(bromomethyl)quinoline has been employed in the synthesis of complex molecules, including pharmaceuticals and materials with potential applications in fields such as medicine and optoelectronics. Its unique chemical properties make it a valuable building block in the construction of novel compounds with specific properties and functions.
