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Chlorotri(1-pyrrolidinyl)phosphonium hexafluorophosphate丨CAS 133894-48-1 Bulk Supplier
Chemical Identifiers
| InChI | InChI=1S/C12H24ClN3P.F6P/c13-17(14-7-1-2-8-14,15-9-3-4-10-15)16-11-5-6-12-16;1-7(2,3,4,5)6/h1-12H2;/q+1;-1 |
| InChI Key | BSCYRXJVGSZNKX-UHFFFAOYSA-N |
| Smiles | C1CCN(C1)[P+](N2CCCC2)(N3CCCC3)Cl.F[P-](F)(F)(F)(F)F |
| EC No. | 628-539-2 |
| MDL No. | MFCD00210035 |
| PubChem CID | 16211753 |
Applications
Peptide Synthesis and Peptide Bond Formation
Phosphonium-based coupling reagents are used in peptide chemistry to facilitate the formation of amide bonds between protected amino acids. Chlorotri(1-pyrrolidinyl)phosphonium hexafluorophosphate may be evaluated in suitable peptide coupling workflows, subject to confirmation of its specific reactivity and compatibility with the target sequence. Researchers should optimize reaction conditions according to substrate properties, protecting-group strategy, and required product quality.
Pharmaceutical Research and Drug Discovery
In pharmaceutical research, coupling reagents support the preparation of amide-containing intermediates and candidate compounds used in medicinal chemistry. This compound may be considered for synthetic route development involving carboxylic acids and amines, provided its identity and reaction performance are verified. Its suitability depends on the molecular structure, functional-group compatibility, and requirements for controlling impurities.
Complex Molecules and Specialty Intermediates
Synthetic Method Development and Laboratory Research
This reagent may be relevant to laboratory-scale reaction screening and synthetic method development. Researchers can investigate reaction parameters and purification strategies to establish reproducible procedures and assess product quality. Because the compound contains a reactive phosphorus–chlorine functionality, appropriate handling, storage, and waste disposal should follow the current Safety Data Sheet and established laboratory safety procedures.

