Triphenylcarbinol

Details

Stereochemistry	ACHIRAL
Molecular Formula	C19H16O
Molecular Weight	260.3297
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=LZTRCELOJRDYMQ-UHFFFAOYSA-N

InChI=1S/C19H16O/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,20H

HIDE SMILES / InChI

Molecular Formula	C19H16O
Molecular Weight	260.3297
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Cyclopropylamines from N,N-dialkylcarboxamides and Grignard reagents in the presence of titanium tetraisopropoxide or methyltitanium triisopropoxide.	2010-12-10	20945442
The rearrangement of the trityloxy radical: Sherlock Holmes' most recent case.	2010-09-17	20648510
Isomerization of triphenylmethoxyl: the Wieland free-radical rearrangement revisited a century later.	2010-08-09	20672259
Enantioselective, iridium-catalyzed monoallylation of ammonia.	2009-08-19	19722644
Direct synthesis of a photoactive inorganic-organic mesostructured hybrid material and its application as a photocatalyst.	2009-05-11	19229898
NMR studies of coupled low- and high-barrier hydrogen bonds in pyridoxal-5'-phosphate model systems in polar solution.	2007-05-16	17455937
N1-substituted thymine derivatives as mitochondrial thymidine kinase (TK-2) inhibitors.	2006-12-28	17181158
Isomerization of triphenylmethoxyl and 1,1-diphenylethoxyl radicals. Revised assignment of the electron-spin resonance spectra of purported intermediates formed during the ceric ammonium nitrate mediated photooxidation of aryl carbinols.	2006-12-22	17168621
Hydrocarbon species mu3-CCH2-, mu3-CCH3 and mu-CHCH3 supported on Ti3O3.	2005-08-07	16027910
Aluminium alkyl complexes supported by [OSSO] type bisphenolato ligands: synthesis, characterization and living polymerization of rac-lactide.	2005-02-21	15702183
Electron impact ionization in helium nanodroplets: controlling fragmentation by active cooling of molecular ions.	2004-09-15	15355110
Photoaddition of water and alcohols to the anthracene moiety of 9-(2'-hydroxyphenyl)anthracene via formal excited state intramolecular proton transfer.	2004-06-30	15212537
Efficient asymmetric synthesis of (S)- and (R)-N-Fmoc-S-trityl-alpha-methylcysteine using camphorsultam as a chiral auxiliary.	2004-06-25	15202920
Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamides.	2003-09-15	12941326
An efficient and large-scale enantioselective synthesis of PNP405: a purine nucleoside phosphorylase inhibitor.	2002-09-20	12227788
Intermolecular interactions in (arene)chromium carbonyl compounds: prediction of chiral crystal packing from racemate structure.	2002-05-08	11982376

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:22:09 GMT 2025` Edited by `admin` on `Mon Mar 31 21:22:09 GMT 2025`
Record UNII	U97Q0OU9KB
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

TRIPHENYLMETHANOL

Preferred Name

English

Triphenylcarbinol

Systematic Name

English

TRIPHENYLCARBINOL [MI]

Common Name

English

NSC-4050

Code

English

HYDROXYTRIPHENYLMETHANE

Systematic Name

English

ZIDOVUDINE IMPURITY D [EP IMPURITY]

Common Name

English

ZIDOVUDINE IMPURITY D [WHO-IP]

Common Name

English

BENZENEMETHANOL, .ALPHA.,.ALPHA.-DIPHENYL-

Systematic Name

English

LOSARTAN POTASSIUM IMPURITY G [EP IMPURITY]

Common Name

English

TRIPHENYLMETHANOL [USP-RS]

Common Name

English

TRITANOL

Systematic Name

English

Code System Code Type Description

PUBCHEM

6457