Ordering
Available Variants10 g
CHA.55727-10g
Price
€82.40
Available – Dispatch in 14 days
50 g
CHA.55727-50g
Price
€291.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.55727-10g | €82.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
50 g | CHA.55727-50g | €291.20 |
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) | C9H6ClNO2 |
|---|---|
| CAS Number | 17564-64-6 |
| Molecular Weight | 195.60 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 24853898 |
| EC Number | 241-541-4 |
| Beilstein/REAXYS Number | 140942 |
| MDL number | MFCD00005898 |
| Assay | 97% |
| Form | powder |
Safety Information Handling visibility
| pictograms |
GHS06
 GHS06
|
|---|---|
| signalword | Danger |
| hcodes | H301,H315,H317,H319,H335 |
| pcodes | P280 - P301 + P310 + P330 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - 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 | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
Technical Overview & Applications Use-case context
N-(Chloromethyl)phthalimide, with the CAS number 17564-64-6, is a chemical compound that has been utilized in various synthetic applications. This compound is a derivative of phthalimide, where a chloromethyl group is attached to the nitrogen atom, imparting unique reactivity. The presence of the chloromethyl group allows for nucleophilic substitution reactions, making it a useful intermediate in the synthesis of more complex molecules. N-(Chloromethyl)phthalimide has been employed in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals, showcasing its versatility as a building block in organic synthesis. Its reactivity and stability under various conditions have made it a valuable compound in the repertoire of synthetic chemists, facilitating the development of new compounds with potential biological and industrial applications.
