Ordering
Available Variants5 g
CHA.41523-5g
Price
€81.60
Available – Dispatch in 14 days
25 g
CHA.41523-25g
Price
€122.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.41523-5g | €81.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.41523-25g | €122.40 |
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) | C6H7NO2 |
|---|---|
| CAS Number | 1193-62-0 |
| Molecular Weight | 125.13 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883091 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00817048 |
| Assay | 97% |
| Form | solid |
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
Methyl 2-pyrrolecarboxylate, with the CAS registry number 1193-62-0, is a chemical compound that has garnered significant attention in various fields of research. This ester derivative of 2-pyrrolecarboxylic acid is a crucial intermediate in the synthesis of numerous pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structural features, including the pyrrole ring and the carboxylate functional group, render it an attractive building block for the construction of complex molecules. The compounds reactivity and versatility have led to its widespread adoption in various synthetic methodologies, including condensation reactions, cyclization reactions, and metal-catalyzed cross-coupling reactions. As a result, methyl 2-pyrrolecarboxylate has become a staple in many chemical laboratories, where it is used to access a diverse range of biologically active compounds and materials with potential applications in medicine, agriculture, and materials science.
