CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
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  • CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
  • CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
  • CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
  • CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
  • CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate
  • CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate

CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate

CAS:98946-18-0 NAME:TBTA tert-Butyl 2,2,2-trichloroacetiMidate MF:C6H10Cl3NO MW:218.51 EINECS:629-631-5 PURITY:98% Appearance:Clear colorless to pale yellow liquid COA:Provide Sample:Negotiable

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Product introduction

PRODUCT NAME  TBTA tert-Butyl 2,2,2-trichloroacetiMidate
CAS NO 98946-18-0
MP 21 °C(lit.)
BP 65 °C11 mm Hg(lit.)
DENSITY 1.222
STORAGE 2-8°C
DELIVERY 2-3DAYS
PACKAGE According client's request

Description of CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate


Tert-butyl 2,2,2-trichloroacetimidate CAS:98946-18-0 is an organic molecule that can be used to synthesize a peptide in a solid-phase synthesis. It reacts with amines and phosphoric acid to form the corresponding ester and trichloroacetamide. This reaction occurs in an acidic environment and does not require any external catalysts. The molecule is stable in the presence of hydrogen fluoride and is not reactive with other nucleophiles. Tert-butyl 2,2,2-trichloroacetimidate has been shown to be useful for the synthesis of cyclic peptides.

 

 


Applications of CAS:98946-18-0 TBTA tert-Butyl 2,2,2-trichloroacetiMidate

1. Catalyst for tert-Butylation of Alcohols and Phenols
tert-Butyl 2,2,2-trichloroacetimidate is used as a tert-butylation reagent, particularly effective in the presence of a noncoordinating acid-base catalyst.

2. Protective Group for Alcohols
3. Conversion of Carbamates
4. Synthesis of α-D-Galactopyranosides and α-D-Glucopyranosides
5. Synthesis of Pharmaceutical Intermediates

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