11625

Di-tert-butyl azodicarboxylate

purum, ≥98.0% (GC)

• Sinónimos: Bis(1,1-dimethylethyl)azodicarboxylate, DBAD, Di-tert-butyl azodiformate, NSC 109889
• Fórmula lineal: (CH₃)₃COCON=NCOOC(CH₃)₃
• Número de CAS: 870-50-8
• Peso molecular: 230.26
• Beilstein: 1911434
• Número CE: 212-796-9
• Número MDL: MFCD00015001
• Código UNSPSC: 12352108
• ID de la sustancia en PubChem: 329749512
• NACRES: NA.22

Propiedades

• grado: purum
• Nivel de calidad: 200
• Ensayo: ≥98.0% (GC)
• Formulario: solid
• mp: 89-92 °C (lit.); 89-92 °C
• grupo funcional: azo
• temp. de almacenamiento: 2-8°C
• cadena SMILES: CC(C)(C)OC(=O)\N=N\C(=O)OC(C)(C)C
• InChI: 1S/C10H18N2O4/c1-9(2,3)15-7(13)11-12-8(14)16-10(4,5)6/h1-6H3/b12-11+
• Clave InChI: QKSQWQOAUQFORH-VAWYXSNFSA-N

Descripción

Descripción general

Di-tert-butyl azodicarboxylate is a an acid labile reagent for Mitsunobu reactions allowing facile isolation of products and for the electrophilic amination and hydrazination of enolates and lithium alkyls.

Aplicación

Reactant for:

• Preparation of hexapeptide key fragments via stereoselective selenocyclization/oxidative deselenylation or hydrazination/cyclization reactions
• Asymmetric Michael addition reactions
• Preparation of dipeptidyl peptidase IV dependent water-soluble prodrugs via Mitsunobu reaction
• Synthesis of pyrroloisoquinoline template via stereoselective N-acyliminium-mediated cyclization and enolate amination for synthesis of peptidomimetic compounds
• Barbier-type propargylation reactions
• Synthesis of bacterial peptide deformylase (PDF) inhibitor fumimycin
• Asymmetric amination of glycine Schiff bases

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: dust mask type N95 (US), Eyeshields, Gloves