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Available Variants1 g
CHA.19252-1g
Price
€118.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.19252-1g | €118.40 |
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) | C8H5Br2N |
|---|---|
| CAS Number | 36132-08-8 |
| Molecular Weight | 274.94 |
| NACRES | NA.22 |
| PubChem Substance ID | 329762825 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD03090642 |
| Assay | 97% |
| Form | powder |
Safety Information Handling visibility
| pictograms |
GHS06
GHS05
  GHS06,GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H301,H315,H318,H335,H413 |
| pcodes | P273 - P280 - P301 + P310 + P330 - P302 + P352 - P305 + P351 + P338 + P310 |
| Hazard Classifications | Acute Tox. 3 Oral - Aquatic Chronic 4 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
5,7-Dibromoindole, with the CAS registry number 36132-08-8, is a halogenated indole derivative that has garnered significant attention in the realm of organic chemistry. This compound is characterized by the presence of two bromine atoms at the 5 and 7 positions of the indole ring, which imparts unique chemical and physical properties. The synthesis of 5,7-dibromoindole typically involves the bromination of indole, and the resulting compound can be further functionalized to yield a wide range of derivatives. These derivatives have been explored for their potential applications in various fields, including pharmaceuticals, materials science, and catalysis. The reactivity of 5,7-dibromoindole towards various nucleophiles and electrophiles makes it a versatile intermediate in the synthesis of complex molecules, and its properties continue to be studied and utilized in ongoing research efforts.
