ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > Oxime > BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Basic information
- Product Name:
- BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
- Synonyms:
-
- BIS(2,2,2-TRICHLOROETHYL) AZODI-CARBOXYL ATE, 97+%
- AZODICARBOXYLIC ACID BIS(2,2,2-TRICHLOROETHYL) ESTER
- BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
- Bis(2,2,2-trichloroethyl) azodicarboxyle
- BEAZ Bis(2,2,2-trichloroethyl) azodicarboxylate
- 1,2-Diazenedicarboxylic acid, 1,2-bis(2,2,2-trichloroethyl) ester
- Bis(2,2,2-
trichloroethyl) azodicarboxylate
- CAS:
- 38857-88-4
- MF:
- C6H4Cl6N2O4
- MW:
- 380.83
- Mol File:
- 38857-88-4.mol
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BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Chemical Properties
- Melting point:
- 109-111 °C (lit.)
- Boiling point:
- 380.7±42.0 °C(Predicted)
- Density
- 1.78±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- BRN
- 2141527
- CAS DataBase Reference
- 38857-88-4
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MSDS
- Language:English Provider:SigmaAldrich
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BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Usage And Synthesis
Chemical Properties
Yellow powder or crystals
Uses
Bis(2,2,2-trichloroethyl) azodicarboxylate has been used:
- in the asymmetric synthesis of substituted cycloalkyl[b]indoles
- as amination reagent during the aza-ene reaction of different alkenes to yield the corresponding allyl amines
- in para-directed amination of C2-alkyl substituted anisole
- in the synthesis of acid- and base-sensitive azo compounds and in Diels-Alder cycloadditions
General Description
Thermal inverse-type hetero-Diels-Alder reaction of O-silyl-protected lactal and bis(2,2,2-trichloroethyl) azodicarboxylate has been reported.
BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATESupplier
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