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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 of TRIPHENYLCARBINOL

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

PubMed

TitleDatePubMed
Efficient asymmetric synthesis of (S)- and (R)-N-Fmoc-S-trityl-alpha-methylcysteine using camphorsultam as a chiral auxiliary.
2004 Jun 25
Photoaddition of water and alcohols to the anthracene moiety of 9-(2'-hydroxyphenyl)anthracene via formal excited state intramolecular proton transfer.
2004 Jun 30
Hydrocarbon species mu3-CCH2-, mu3-CCH3 and mu-CHCH3 supported on Ti3O3.
2005 Aug 7
Aluminium alkyl complexes supported by [OSSO] type bisphenolato ligands: synthesis, characterization and living polymerization of rac-lactide.
2005 Feb 21
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 Dec 22
N1-substituted thymine derivatives as mitochondrial thymidine kinase (TK-2) inhibitors.
2006 Dec 28
Enantioselective, iridium-catalyzed monoallylation of ammonia.
2009 Aug 19
Isomerization of triphenylmethoxyl: the Wieland free-radical rearrangement revisited a century later.
2010 Aug 9
Cyclopropylamines from N,N-dialkylcarboxamides and Grignard reagents in the presence of titanium tetraisopropoxide or methyltitanium triisopropoxide.
2010 Dec 10
The rearrangement of the trityloxy radical: Sherlock Holmes' most recent case.
2010 Sep 17
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:28:52 GMT 2023
Edited
by admin
on Sat Dec 16 04:28:52 GMT 2023
Record UNII
U97Q0OU9KB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIPHENYLCARBINOL
MI  
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
TRIPHENYLMETHANOL
Systematic 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
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-988-5
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
MERCK INDEX
m11182
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
TRIPHENYLMETHANOL
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID0058803
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
RS_ITEM_NUM
1695343
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
FDA UNII
U97Q0OU9KB
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
CAS
76-84-6
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
NSC
4050
Created by admin on Sat Dec 16 04:28:52 GMT 2023 , Edited by admin on Sat Dec 16 04:28:52 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
UNSPECIFIED
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
Not Specified
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP