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Available Variants10 g
CHA.81303-10g
Price
€98.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.81303-10g | €98.40 |
98%
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) | C6H5ClN2O3 |
|---|---|
| CAS Number | 38533-61-8 |
| Molecular Weight | 188.57 |
| NACRES | NA.22 |
| PubChem Substance ID | 24892744 |
| UNSPSC Code | 12352100 |
| EC Number | 253-989-8 |
| MDL number | MFCD00130268 |
| Assay | 98% |
| Form | powder |
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
2-Chloro-6-methoxy-3-nitropyridine, with the CAS registry number 38533-61-8, is a synthetic organic compound that belongs to the pyridine family. It is characterized by the presence of a chlorine atom at the 2-position, a methoxy group at the 6-position, and a nitro group at the 3-position of the pyridine ring. This compound exhibits unique chemical and physical properties, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the electron-withdrawing nitro group and the electron-donating methoxy group, which can participate in various chemical reactions, such as nucleophilic substitution and electrophilic aromatic substitution. The compounds properties and reactivity make it a useful building block in the development of new chemicals with potential biological activity.
