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108545

Sigma-Aldrich

4-Tritylphenol

97%

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About This Item

Linear Formula:
(C6H5)3CC6H4OH
CAS Number:
978-86-9
Molecular Weight:
336.43
EC Number:
213-557-1
MDL number:
MFCD00002364
UNSPSC Code:
12352100
PubChem Substance ID:
24846810
NACRES:
NA.22

Quality Level

100

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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