11625

Azodicarbonsäure-di-tert.-butylester

purum, ≥98.0% (GC)

• Synonym(e): Bis(1,1-dimethylethyl)azodicarboxylate, DBAD, Di-tert-butyl azodiformate, NSC 109889
• Lineare Formel: (CH₃)₃COCON=NCOOC(CH₃)₃
• CAS-Nummer: 870-50-8
• Molekulargewicht: 230.26
• Beilstein: 1911434
• EG-Nummer: 212-796-9
• MDL-Nummer: MFCD00015001
• UNSPSC-Code: 12352108
• PubChem Substanz-ID: 329749512
• NACRES: NA.22

Eigenschaften

• Qualität: purum
• Qualitätsniveau: 200
• Assay: ≥98.0% (GC)
• Form: solid
• mp (Schmelzpunkt): 89-92 °C (lit.); 89-92 °C
• Funktionelle Gruppe: azo
• Lagertemp.: 2-8°C
• SMILES String: 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+
• InChIKey: QKSQWQOAUQFORH-VAWYXSNFSA-N

Beschreibung

Allgemeine Beschreibung

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.

Anwendung

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

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Gloves