BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE

BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
  • CAS No.:38857-88-4

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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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 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 Reference38857-88-4
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Usage And Synthesis
Chemical PropertiesYellow powder or crystals
UsesBis(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 DescriptionThermal 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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