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| 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 | CAS: | 38857-88-4 | MF: | C6H4Cl6N2O4 | MW: | 380.83 | EINECS: | | Product Categories: | | Mol File: | 38857-88-4.mol | ![BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Structure](CAS/GIF/38857-88-4.gif) |
| 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 |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | WGK Germany | 3 |
| 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) AZODICARBOXYLATE Preparation Products And Raw materials |
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