11625

Di-tert-butyl azodicarboxylate

purum, ≥98.0% (GC)

• Synonyme(s) : Bis(1,1-dimethylethyl)azodicarboxylate, DBAD, Di-tert-butyl azodiformate, NSC 109889
• Formule linéaire : (CH₃)₃COCON=NCOOC(CH₃)₃
• Numéro CAS: 870-50-8
• Poids moléculaire : 230.26
• UNSPSC Code: 12352108
• NACRES: NA.22
• PubChem Substance ID: 329749512
• EC Number: 212-796-9
• Beilstein/REAXYS Number: 1911434
• MDL number: MFCD00015001
• Assay: ≥98.0% (GC)
• Form: solid

Propriétés

• grade: purum
• Quality Segment: 200
• assay: ≥98.0% (GC)
• form: solid
• mp: 89-92 °C
• functional group: azo
• storage temp.: 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+
• InChI key: QKSQWQOAUQFORH-VAWYXSNFSA-N

Description

General description

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.

Application

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

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves