Ordering
Available Variants5 g
CHA.27226-5g
Price
€120.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.27226-5g | €120.00 |
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) | C5H3ClO2S |
|---|---|
| CAS Number | 59337-89-2 |
| Molecular Weight | 162.59 |
| NACRES | NA.22 |
| PubChem Substance ID | 24881149 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00043888 |
| 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
3-Chlorothiophene-2-carboxylic acid, with the CAS registry number 59337-89-2, is a chemical compound that belongs to the class of thiophene derivatives. This compound exhibits a molecular structure consisting of a thiophene ring with a chloro substituent at the 3-position and a carboxylic acid group at the 2-position. The physical and chemical properties of 3-chlorothiophene-2-carboxylic acid make it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its reactivity towards various functional groups and its ability to undergo different types of chemical reactions, such as esterification and amidation, render it a versatile building block in organic synthesis. The compounds properties and reactivity have been extensively studied, and it has been employed in the preparation of a range of biologically active molecules.
