Ordering
Available Variants5 mg
CHA.92342-5mg
Price
€85.60
Available – Dispatch in 14 days
25 mg
CHA.92342-25mg
Price
€326.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mg | CHA.92342-5mg | €85.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 mg | CHA.92342-25mg | €326.40 |
chromogenic, ≥97%, powder
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) | C14H15BrClNO6 |
|---|---|
| CAS Number | 15548-60-4 |
| Molecular Weight | 408.63 |
| NACRES | NA.83 |
| PubChem Substance ID | 24891784 |
| UNSPSC Code | 12352204 |
| EC Number | 239-603-0 |
| MDL number | MFCD00063690 |
| Beilstein/REAXYS Number | 1552603 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside, with the CAS number 15548-60-4, is a synthetic compound that has been utilized in various biochemical and pharmacological studies. This molecule consists of an indole backbone substituted with bromo and chloro groups, which is further conjugated to a β-D-glucopyranoside moiety. The unique structure of this compound makes it a valuable tool for investigating various biological processes, including enzyme-substrate interactions and glycoside metabolism. Researchers have employed this compound to study the activity of specific enzymes, such as β-glucosidases, and to develop novel assays for detecting these enzymes. The compounds properties and reactivity have also been explored in the context of medicinal chemistry and drug discovery, highlighting its potential as a lead molecule for the development of new therapeutic agents.
