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Details

Stereochemistry ACHIRAL
Molecular Formula C19H15Cl
Molecular Weight 278.775
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Chlorotriphenylmethane

SMILES

ClC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=JBWKIWSBJXDJDT-UHFFFAOYSA-N
InChI=1S/C19H15Cl/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

HIDE SMILES / InChI
Molecular Formula C19H15Cl
Molecular Weight 278.775
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Covalency in Ce(IV) and U(IV) halide and N-heterocyclic carbene bonds.
2010-08-16
Preparation of 6beta-estradiol derivative libraries as bisubstrate inhibitors of 7beta-hydroxysteroid dehydrogenase type using the multidetachable sulfamate linker.
2010-03-10
Synthesis of Peptides from α- and β-Tubulin Containing Glutamic Acid Side-Chain Linked Oligo-Glu with Defined Length.
2010
Triphenyl-methyl benzoate.
2009-07-29
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Diethyl 2-(triphenyl-meth-yl)malonate.
2008
Homogeneous tritylation of cellulose in 1-butyl-3-methylimidazolium chloride.
2007-04-10
Pediatric susceptibility to 18 industrial chemicals: a comparative analysis of newborn with young animals.
2007-04
First protection of a wide-rim tetraamino calix[4]arene in opposite positions.
2007-03-15
[Life and death of free radicals].
2007-01
Synthesis of libraries of 16beta-aminopropyl estradiol derivatives for targeting two key steroidogenic enzymes.
2006-11
Oxidation studies on Andrographolide.
2006-10
Mild and adaptable silver triflate-assisted method for trityl protection of alcohols in solution with solid-phase loading applications.
2006-08-31
Comparative susceptibility of newborn and young rats to six industrial chemicals.
2005-12
Preparation and evaluation of trimethylsilylated chitin as a versatile precursor for facile chemical modifications.
2005-05-10
An NQR study of the polymorphism of triphenylchloromethane.
2004-01
Solid-phase parallel synthesis of 17alpha-substituted estradiol sulfamate and phenol libraries using the multidetachable sulfamate linker.
2003-07-15
An efficient and large-scale enantioselective synthesis of PNP405: a purine nucleoside phosphorylase inhibitor.
2002-09-20
Molecular "compasses" and "gyroscopes". I. Expedient synthesis and solid state dynamics of an open rotor with a bis(triarylmethyl) frame.
2002-03-20
Cationic host-guest polymerization of N-vinylcarbazole and vinyl ethers in MCM-41, MCM-48, and nanoporous glasses.
2001-09-03
Trityl isothiocyanate support for solid-phase synthesis.
2001-01-10
Patents

Patents

04154959
3
04189597
3
04202822
3
04259324
1
04331665
2
04463173
1
04476122
1
04526977
1
04640925
1
04661489
1
04666633
1
04694076
1
04762942
1
04861769
4
04889861
4
04933355
9
05037842
1
05049551
3
05175166
1
05198208
8
05233031
2
05234936
1
05280032
2
05290780
2
05298494
1
05332831
5
05403845
1
05420122
2
05438145
1
05463073
1
05525720
1
05534639
2
05574051
2
05665881
2
05817678
1
05877312
1
05955487
2
05972942
1
05977374
2
06020317
1
06040480
2
06051712
73
06060038
1
06077853
2
JP5315866B2
1
JPH01268686A
1
JPH01308294A
1
JPH02231462A
1
JPH09299086A
1
JPH10316686A
1
JPS52136157A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:54:02 GMT 2025
Edited
by admin
on Mon Mar 31 17:54:02 GMT 2025
Record UNII
1D9GZ8QQXN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Trityl chloride
MI  
Preferred Name English
Chlorotriphenylmethane
Systematic Name English
Triphenylchloromethane
Systematic Name English
Trityl chloride [MI]
Common Name English
Triphenylmethyl chloride
Systematic Name English
TPCM
Common Name English
NSC-435
Code English
Benzene, 1,1',1"-(chloromethylidyne)tris-
Systematic Name English
Methane, chlorotriphenyl-
Systematic Name English
Code System Code Type Description
MERCK INDEX
m11214
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID3052511
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
WIKIPEDIA
Triphenylmethyl chloride
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
HSDB
2807
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-986-4
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
CAS
76-83-5
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
PUBCHEM
6456
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
NSC
435
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
FDA UNII
1D9GZ8QQXN
Created by admin on Mon Mar 31 17:54:02 GMT 2025 , Edited by admin on Mon Mar 31 17:54:02 GMT 2025
PRIMARY
NIH
NCATS
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