Ordering
Available Variants1 g
CHA.26671-1g
Price
€44.16
Available – Dispatch in 14 days
5 g
CHA.26671-5g
Price
€93.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.26671-1g | €44.16 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.26671-5g | €93.60 |
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) | C5H4N2S |
|---|---|
| CAS Number | 4651-82-5 |
| Molecular Weight | 124.16 |
| NACRES | NA.22 |
| PubChem Substance ID | 24885613 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00706298 |
| Assay | 97% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302,H315,H318,H335 |
| pcodes | P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Dam. 1 - 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, Faceshields, Gloves |
Technical Overview & Applications Use-case context
2-Aminothiophene-3-carbonitrile, with the CAS registry number 4651-82-5, is a chemical compound that has garnered significant attention in the realm of organic chemistry. This compound is characterized by its thiophene ring, which is a five-membered heterocyclic structure containing sulfur, and is further functionalized with an amino group and a nitrile group at the 2 and 3 positions, respectively. The presence of these functional groups imparts unique chemical properties to the compound, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compounds reactivity and versatility have led to its widespread use in various chemical transformations, including cross-coupling reactions and nucleophilic substitutions, allowing chemists to access a diverse range of complex molecules. As such, 2-aminothiophene-3-carbonitrile is an important building block in modern organic synthesis.
