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It is usually bound to a molecule, but can exist as a stable cation in solution, where it appears bright orange.
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277:"Dimethoxytrityl Removal in Organic Medium: Efficient Oligonucleotide Synthesis Without Chlorinated Solvents"
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InChI=1S/C21H20O2/c1-22-19-12-8-17(9-13-19)21(16-6-4-3-5-7-16)18-10-14-20(23-2)15-11-18/h3-15,21H,1-2H3
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Except where otherwise noted, data are given for materials in their
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Krotz, Achim; Cole, Douglas; Ravikumar, Vasulinga (1999).
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widely used for protection of the 5'-hydroxy group in
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184:COC1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=C(C=C3)OC
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40:bis(4-methoxyphenyl)-phenylmethyl radical
60:Bis(p-methoxyphenyl)phenylmethyl radical
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163:Key: RIRAVPPUGSNYOU-UHFFFAOYSA-N
57:4,4'-Dimethoxytriphenylmethyl radical
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225:(at 25 °C , 100 kPa).
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281:Nucleosides and Nucleotides
54:4,4'-Dimethoxytrityl cation
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293:10.1080/07328319908044664
253:oligonucleotide synthesis
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51:4,4'-Benzylidenedianisole
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311:Molecule of the Day
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287:(6–7): 1207–1209.
251:, particularly in
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338:Protecting groups
237:Chemical compound
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113:Interactive image
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200:Chemical formula
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315:. Retrieved
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72:Identifiers
46:Other names
249:nucleosides
193:Properties
317:2022-05-03
262:References
211:Molar mass
100:3D model (
79:CAS Number
37:IUPAC name
89:7500-76-7
332:Category
125:PubChem
177:SMILES
31:Names
152:InChI
138:82012
102:JSmol
289:doi
128:CID
63:DMT
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