Ordering
Available Variants1 g
CHA.58295-1g
Price
€31.92
Available – Dispatch in 14 days
5 g
CHA.58295-5g
Price
€66.96
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.58295-1g | €31.92 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.58295-5g | €66.96 |
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) | C9H6BrNO |
|---|---|
| CAS Number | 877-03-2 |
| Molecular Weight | 224.05 |
| NACRES | NA.22 |
| PubChem Substance ID | 24874042 |
| UNSPSC Code | 12352100 |
| EC Number | 212-884-7 |
| MDL number | MFCD00152016 |
| Assay | 98% |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | 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
5-Bromoindole-3-carboxaldehyde, with the CAS registry number 150255-96-2, is a chemical compound that has garnered significant attention in the realm of organic chemistry. This compound is a derivative of indole, a heterocyclic aromatic organic compound, and features a bromine atom at the 5-position and an aldehyde functional group at the 3-position. The unique combination of these functional groups renders 5-Bromoindole-3-carboxaldehyde a valuable intermediate in the synthesis of various complex molecules, including pharmaceuticals and materials science applications. Its reactivity and versatility make it an attractive starting material for a range of chemical transformations, including condensation reactions and cross-coupling reactions, allowing for the creation of diverse molecular structures with potential biological and technological significance.
