| Identification | Back Directory | [Name]
Potassium 5-hydroxypentanoyltrifluoroborate | [CAS]
1370291-68-1 | [Synonyms]
ium 5-hydroxypentanoyltrifluoroborate
Potassium 5-hydroxypentanoyltrifluoroborate | [Molecular Formula]
C5H9BF3KO2 | [MDL Number]
MFCD22417242 | [MOL File]
1370291-68-1.mol | [Molecular Weight]
208.03 |
| Chemical Properties | Back Directory | [Melting point ]
123.6°C | [form ]
powder | [InChI]
1S/C5H9BF3O2.K/c7-6(8,9)5(11)3-1-2-4-10;/h10H,1-4H2;/q-1;+1 | [InChIKey]
OLLDPQQFLCSTQN-UHFFFAOYSA-N | [SMILES]
[K+].OCCCCC(=O)[B-](F)(F)F |
| Safety Data | Back Directory | [WGK Germany ]
WGK 3 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
Potassium Acyltrifluroborates (KATs) are bench, air and moisture stable reagents for rapid, chemoselective amide bond formations with hydroxylamines. These amide bond forming reactions proceed under aqueous conditions, without the need for coupling reagents or protecting groups. This product was introduced in collaboration with the Bode Research Group. | [General Description]
Potassium 5-hydroxypentanoyltrifluoroborate belongs to the class of compounds known as potassium acyltrifluroborates (KATs). It acts as an acyl donor during the amidation of O-benzoyl hydroxylamine to form the corresponding amide product. |
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