Ordering
Available Variants1 g
CHA.58791-1g
Price
€85.80
Available – Dispatch in 14 days
5 g
CHA.58791-5g
Price
€287.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.58791-1g | €85.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.58791-5g | €287.20 |
99%
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) | C10H7BrO |
|---|---|
| CAS Number | 30478-88-7 |
| Molecular Weight | 223.07 |
| NACRES | NA.22 |
| PubChem Substance ID | 329761316 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD10000951 |
| Assay | ≥98.5% (HPLC), 99% |
| Form | powder |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H315,H318,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Dam. 1 - 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
3-Bromo-2-naphthol, with the CAS registry number 30478-88-7, is a chemical compound that belongs to the naphthol family. It is a white crystalline solid with a molecular formula of C10H7BrO and a molecular weight of 221.07 g/mol. This compound is used as an intermediate in the synthesis of various pharmaceuticals, dyes, and pigments. The bromine substituent at the 3-position of the naphthol ring makes it a versatile building block for further chemical transformations. 3-Bromo-2-naphthol can undergo various reactions, including nucleophilic substitution, electrophilic substitution, and metal-catalyzed cross-coupling reactions, making it a valuable precursor for the synthesis of complex molecules. Its properties and reactivity make it a useful compound in various fields of chemistry, including medicinal chemistry, materials science, and organic synthesis.
