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About This Item
Linear Formula:
(C6H5)3CC6H4OH
CAS Number:
Molecular Weight:
336.43
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
283-286 °C (lit.)
SMILES string
Oc1ccc(cc1)C(c2ccccc2)(c3ccccc3)c4ccccc4
InChI
1S/C25H20O/c26-24-18-16-23(17-19-24)25(20-10-4-1-5-11-20,21-12-6-2-7-13-21)22-14-8-3-9-15-22/h1-19,26H
InChI key
NIPKXTKKYSKEON-UHFFFAOYSA-N
Related Categories
Application
4-Tritylphenol was used in the synthesis of 5-arylethynyl-2′-deoxyuridines and propargyl ethers. It may be used in the synthesis of pyridyl rotaxane.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Bilge Baytekin et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(32), 10012-10028 (2008-10-01)
Tetralactam macrocycles can be functionalized by a variety of cross-coupling reactions. A modular "toolbox" strategy is presented that allows 1) several tetralactam macrocycles to be covalently connected with each other or with a central spacer, 2) the macrocycles to be
Mikhail V Skorobogatyi et al.
Organic & biomolecular chemistry, 4(6), 1091-1096 (2006-03-10)
Three new 5-arylethynyl-2'-deoxyuridines containing bulky aryls have been prepared and tested against HSV-1 in Vero cells. The introduction of a substituent in the phenyl group of an inactive compound, 5-phenylethynyl-2'-deoxyuridine, leads to the appearance of anti-HSV properties. The most active
Christopher Elam et al.
European journal of medicinal chemistry, 46(5), 1512-1523 (2011-03-01)
Two screening protocols based on recursive partitioning and computational ligand docking methodologies, respectively, were employed for virtual screens of a compound library with 345,000 entries for novel inhibitors of the enzyme sarco/endoplasmic reticulum calcium ATPase (SERCA), a potential target for
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