| Weight | 278.782 g/mol |
|---|---|
| Formula | C19H15Cl |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Trityl chloride (76-83-5)
triphenylmethylchloride
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- Trityl Chloride as a Novel and Efficient Organic Catalyst For Room Temperature Preparation of Bis(indolyl)methanes under Solvent-Free Conditions in Neutral Media (Synthesis, 2008)
- Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature (Applied Catalysis A-general, 2010)
- Organocatalyst trityl chloride efficiently promoted the solvent-free synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-ones by in situ formation of carbocationic system in neutral media (Catalysis Communications, 2012)
- Discovery of an in situ carbocationic system using trityl chloride as a homogeneous organocatalyst for the solvent-free condensation of -naphthol with aldehydes and amides/thioamides/alkyl carbamates in neutral media (Tetrahedron, 2013)
- Electrostatic catalysis of ionic aggregates. I. Ionization and dissociation of trityl chloride and hydrogen chloride in lithium perchlorate-diethyl ether solutions (Journal of the American Chemical Society, 1970)
- Dialkyl aluminium chloride: a reagent for removal of trityl group from trityl ethers of deoxynucleosides, deoxynucleotides, and oligodeoxynucleotides (Tetrahedron Letters, 1982)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - triphenylmethylchloride
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SMILESC1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)Cl
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InChIKeyJBWKIWSBJXDJDT-UHFFFAOYSA-N
- Pubchem - Trityl chloride
- Wikipedia - Triphenylmethyl chloride
Triphenylmethyl chloride or trityl chloride (TrCl) is a white solid with the chemical formula C19H15Cl. It is an alkyl halide, sometimes used to introduce the trityl protecting group.
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Trityl chloride
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