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Available Variants1 g
CHA.23764-1g
Price
€57.52
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.23764-1g | €57.52 |
95%
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) | C6H3BrN2S |
|---|---|
| CAS Number | 1753-75-9 |
| Molecular Weight | 215.07 |
| NACRES | NA.22 |
| PubChem Substance ID | 329767096 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00460091 |
| Assay | 95% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302,H319 |
| pcodes | P264 - P280 - P301 + P312 - P305 + P351 + P338 - P337 + P313 - P501 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Irrit. 2 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
5-Bromo-2,1,3-benzothiadiazole, with the CAS number 1753-75-9, is a chemical compound that belongs to the benzothiadiazole class. This compound exhibits a molecular structure consisting of a benzene ring fused to a thiadiazole ring, with a bromine atom substituted at the 5-position. The presence of the bromine atom imparts unique chemical and physical properties to the compound, making it useful in various applications. 5-Bromo-2,1,3-benzothiadiazole is utilized as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity and versatility make it a valuable building block in organic synthesis, allowing chemists to introduce the benzothiadiazole moiety into complex molecules. The compounds properties and reactivity are well-documented, facilitating its use in a range of chemical transformations and applications.
