Ordering
Available Variants1 g
CHA.87122-1g
Price
€112.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.87122-1g | €112.00 |
≥99.0% (TLC)
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) | C13H18N2O4 |
|---|---|
| CAS Number | 117142-26-4 |
| Molecular Weight | 266.29 |
| UNSPSC Code | 12352209 |
| NACRES | NA.22 |
| PubChem Substance ID | 57647265 |
| MDL number | MFCD00079681 |
| Beilstein/REAXYS Number | 7625087 |
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
Boc-3-(3-pyridyl)-Ala-OH, with the CAS number 117142-26-4, is a synthetic amino acid derivative that has garnered significant attention in the realm of organic chemistry and pharmaceutical research. This compound is characterized by the presence of a pyridine ring attached to the beta carbon of the alanine backbone, which is further protected by a tert-butoxycarbonyl (Boc) group. The incorporation of the pyridine moiety imparts unique chemical and biological properties to the molecule, making it a valuable intermediate in the synthesis of various biologically active compounds, including pharmaceuticals and agrochemicals. The Boc protection allows for the selective deprotection and further functionalization of the amino group, rendering Boc-3-(3-pyridyl)-Ala-OH a versatile building block in peptide and heterocyclic chemistry. Its applications span across multiple disciplines, including medicinal chemistry and materials science.
