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4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID&

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4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID& Basic information

Product Name:
4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID&
Synonyms:
  • 4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID&
  • 2,2,2-Trichloroacetimidic Acid 4-Methoxybenzyl Ester
  • 4-Methoxybenzyl 2,2,2-Trichloroacetimidate
  • 4-Methoxybenzyl trichloroacetimidate
  • 4-methoxybenzyl 2,2,2-trichloroethanimidoate
  • 4-Methoxybenzyl trichloroacetamidate
  • 4-Methoxybenzyl2,2,2-Trichloroacetimidate>
  • 2,2,2-trichlorohydrin-4-methoxybenzyl ester per acetic acid
CAS:
89238-99-3
MF:
C10H10Cl3NO2
MW:
282.55
Product Categories:
  • Others
  • Protecting and Derivatizing Reagents
  • Protection & Derivatization Reagents (for Synthesis)
  • Synthetic Organic Chemistry
  • Protection and Derivatization
Mol File:
89238-99-3.mol
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4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID& Chemical Properties

Boiling point:
137 °C / 0.7mmHg
Density 
1.361 g/mL at 25 °C
refractive index 
n20/D 1.5488
Flash point:
110 °C
storage temp. 
2-8°C
pka
1.96±0.70(Predicted)
form 
clear liquid
color 
Colorless to Light yellow to Light orange
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Safety Information

Hazard Codes 
Xn,N
Risk Statements 
20/21/22-36/37/38-51/53
Safety Statements 
26-61-36/37
RIDADR 
UN 3082 9/PG 3
WGK Germany 
3
HS Code 
29252900
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4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID& Usage And Synthesis

Uses

4-Methoxybenzyl-2,2,2-trichloroacetimidate can be used as a reagent for the protection of alcohols as the p-methoxybenzyl ether. 1o, 2o, and 3o alcohols can be easily protected using this reagent with equal efficiency in the presence of a variety of different protective groups. This reagent is commonly used under acidic conditions therefore it offers an alternative method to the Williamson ether synthesis, which is typically used basic conditions to protect base-sensitive alcohols.

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

4-METHOXYBENZYL-2,2,2-TRICHLOROACETIMID&Supplier

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