Weight | 211.859 g/mol |
---|---|
Formula | C3H2Cl4O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
2,2,2-Trichloroethyl chloroformate (17341-93-4)
trichloroethyl chloroformate
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- 2,2,2-trichloroethyl chloroformate: A general reagent for demethylation of tertiary methylamines (Tetrahedron Letters, 1974)
- Gas chromatography/mass spectrometry determination of amphetaminerelated drugs and ephedrines in plasma, urine and hair samples after derivatization with 2,2,2trichloroethyl chloroformate (Rapid Communications in Mass Spectrometry, 2005)
- Gas chromatographic-mass spectrometric identification and quantification of aniline after extraction from serum and derivatization with 2,2,2-trichloroethyl chloroformate, a novel derivative (Journal of Chromatography B: Biomedical Sciences and Applications, 1998)
- Determination of pethidine in plasma by electron capture gas chromatography after reaction with trichloroethyl chloroformate. (Journal of Chromatography A, 1976)
- Gas chromatography/mass spectrometry determination of mephedrone in drug seizures after derivatization with 2,2,2-trichloroethyl chloroformate. (Rapid Communications in Mass Spectrometry, 2011)
- A rapid novel derivatization of amphetamine and methamphetamine using 2,2,2-trichloroethyl chloroformate for gas chromatography electron ionization and chemical ionization mass spectrometric analysis (American Journal of Clinical Pathology, 1998)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - trichloroethyl chloroformate
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SMILESC(C(Cl)(Cl)Cl)OC(=O)Cl
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InChIKeyLJCZNYWLQZZIOS-UHFFFAOYSA-N
- Pubchem - 2,2,2-Trichloroethyl chloroformate
- Wikipedia - 2,2,2-Trichlorethoxycarbonyl chloride
Trichloroethyl chloroformate is used in organic synthesis for the introduction of the trichloroethyl chloroformate (Troc) protecting group for amines, thiols and alcohols. It readily cleaves vs other carbamates and can be used in an overall protecting group strategy. The troc group is traditionally removed via Zn insertion in the presence of acetic acid, resulting in elimination and decarboxylation.
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