Ordering
Available Variants5 g
CHA.91503-5g
Price
€167.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.91503-5g | €167.40 |
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) | C9H5Cl2N |
|---|---|
| CAS Number | 7742-73-6 |
| Molecular Weight | 198.05 |
| NACRES | NA.22 |
| PubChem Substance ID | 24862933 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00034750 |
| Assay | 97% |
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
1,3-Dichloroisoquinoline, with the CAS number 7742-73-6, is a chemical compound that belongs to the isoquinoline family. It is a pale yellow crystalline solid with a molecular formula of C9H5Cl2N. This compound is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The dichloro substitution pattern on the isoquinoline ring makes it a versatile building block for the preparation of more complex molecules. 1,3-Dichloroisoquinoline is also used in research applications, particularly in the field of medicinal chemistry, where it serves as a precursor for the synthesis of biologically active compounds. Its reactivity and stability under various reaction conditions make it a valuable intermediate in organic synthesis, allowing for the creation of a wide range of derivatives with potential therapeutic properties.
