| Appearance | N/A |
| Content of Zinc | N/A |
| Boiling Point | N / A |
| Melting Point | 33°C |
| Vapor Pressure | N/A |
| % Volatile by Weight | N/A |
| Solubility in Water | N/A |
| Density | N/A |
| pH of Liquid, Typical (10% soln) | N/A |
| Specific Gravity Approx | N/A |
| Odor | N/A |
| pH | N/A |
| Flash Point | N/A |
| Ignition temperature | N/A |
| Lower exposure limit | N/A |
| Upper exposure limit | N/A |
| Color | White-Yellow |
| Linear Formula | C10H16O2N2 |
| Formula Weight | 196.25 |
| Physical Form | Crystal-lump at 20°C |
| Chemical Name or Material | (S)-1-(tert-Butoxycarbonyl)-2-cyanopyrrolidine |
| Molecular Weight | 196.25 g/mol |
| CAS Number | 228244-04-0 |
| Applications | DPP-4 inhibitor drug manufacturing — Boc-2-cyanopyrrolidine building blocks of this type are the standard synthetic precursors to nitrile-based dipeptidyl peptidase-4 (DPP-4) inhibitors, a major class of type 2 diabetes drugs (e.g., vildagliptin-class chemistry) |
This compound is a pyrrolidine ring bearing a Boc (tert-butoxycarbonyl) protecting group and a nitrile substituent, with defined (S)-stereochemistry. The nitrile-pyrrolidine motif, once deprotected, is a hallmark structural feature of nitrile-class DPP-4 inhibitor drugs used to treat type 2 diabetes.
This compound is used as a chiral building block in pharmaceutical manufacturing, particularly for constructing nitrile-based DPP-4 inhibitor active pharmaceutical ingredients after Boc deprotection.
PPE: Standard laboratory precautions — gloves, eyeshields, dust mask
No related products found.
Mainly as a chiral building block in pharmaceutical manufacturing, particularly nitrile-class DPP-4 inhibitor (type 2 diabetes drug) synthesis.
It's a pyrrolidine (5-membered ring) — Sarchem's page title currently says "piperidine," but the CAS number and all published data confirm the pyrrolidine structure. See Critical Finding #7.
Yes, for every lot (SKU S2906).