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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

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

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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