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Details

Stereochemistry ACHIRAL
Molecular Formula C13H12
Molecular Weight 168.2344
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Diphenylmethane

SMILES

C(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=CZZYITDELCSZES-UHFFFAOYSA-N
InChI=1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2

HIDE SMILES / InChI

Molecular Formula C13H12
Molecular Weight 168.2344
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis, biological evaluation, and binding mode of novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles targeted at the HIV-1 reverse transcriptase.
2002-04-11
Oxygen transfer reactions. 4. Reaction of high valent oxoruthenium compounds with sulfides.
2002-04-08
Differential enhancement of dialysate serotonin levels in distinct brain regions of the awake rat by modafinil: possible relevance for wakefulness and depression.
2002-04-01
Development of long-acting dopamine transporter ligands as potential cocaine-abuse therapeutic agents: chiral hydroxyl-containing derivatives of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine.
2002-03-14
Is psychosis exacerbated by modafinil?
2002-03
Pharmacotherapy of the overactive bladder and advances in drug delivery.
2002-03
Muscarinic receptor antagonist-induced lenticular opacity in rats.
2002-03
Determination of modafinil, modafinil acid and modafinil sulfone in human plasma utilizing liquid-liquid extraction and high-performance liquid chromatography.
2002-02-15
Medication update.
2002-02
Effect of modafinil at steady state on the single-dose pharmacokinetic profile of warfarin in healthy volunteers.
2002-02
On the prodrug potential of novel aldose reductase inhibitors with diphenylmethyleneaminooxycarboxylic acid structure.
2002-02
Efficacy and safety of modafinil (Provigil) for the treatment of fatigue in multiple sclerosis: a two centre phase 2 study.
2002-02
Modafinil for fatigue in multiple sclerosis.
2002-02
Reduction of daytime sleepiness in a depressive patient during adjunct treatment with modafinil.
2002-01-05
Maintaining alertness and performance during sleep deprivation: modafinil versus caffeine.
2002-01
Effect of modafinil on the pharmacokinetics of ethinyl estradiol and triazolam in healthy volunteers.
2002-01
[The drop in toxicity and the rise in the effectiveness of antineoplastic chemotherapy by correcting the activity of liver monooxygenases: from the experiment to the clinical practice].
2002
Sleepless in America.
2001-12-17
A novel, tunable manganese coordination system based on a flexible "spacer" unit: noncovalent templation effects.
2001-12-05
Cost-Effectiveness of tolterodine for patients with urge incontinence who discontinue initial therapy with oxybutynin: a Canadian perspective.
2001-12
Is tolterodine (Detrol) or oxybutynin (Ditropan) the best for treatment of urge urinary incontinence?
2001-12
Modafinil: a gift to portmanteau.
2001-11-20
Variations in extracellular monoamines in the prefrontal cortex and medial hypothalamus after modafinil administration: a microdialysis study in rats.
2001-11-16
Palladium-catalyzed asymmetric diene cyclization/hydrosilylation employing functionalized silanes and disiloxanes.
2001-11-16
The importance of residues in substrate recognition site 3 for the catalytic function of CYP2D25 (vitamin D 25-hydroxylase).
2001-11-09
Modafinil as adjunct therapy for daytime sleepiness in obstructive sleep apnea.
2001-11-01
The effect of tolterodine on the pharmacokinetics and pharmacodynamics of a combination oral contraceptive containing ethinyl estradiol and levonorgestrel.
2001-11
Tolterodine: an overview.
2001-11
Tolterodine once-daily in treatment of the overactive bladder.
2001-11
Medical treatment of overactive bladder.
2001-11
Application of different RP-HPLC methods for the determination of the octanol/water partition coefficient of selected tetrachlorobenzyltoluenes.
2001-11
Reference scales for the characterization of cationic electrophiles and neutral nucleophiles.
2001-10-03
Evidence for the efficacy and safety of tolterodine in the treatment of overactive bladder.
2001-10
Engineering the CYP101 system for in vivo oxidation of unnatural substrates.
2001-10
Tolterodine: a clinical review.
2001-10
POEMS (patient-oriented evidence that matters) spark discussion.
2001-10
[Effect of phencarol on pancreatic digestive enzymes in food anaphylaxis].
2001-09-18
Rational design and synthesis of novel 2,5-disubstituted cis- and trans-piperidine derivatives exhibiting differential activity for the dopamine transporter.
2001-09-03
Tolterodine reduces the number of urge incontinence episodes in patients with an overactive bladder.
2001-09
Physiologically based pharmacokinetic model for tetrachlorobenzyltoluenes in rat: comparison of in vitro and in vivo metabolic rates.
2001-09
Resonance Rayleigh scattering study of the interaction of heparin with some basic diphenyl naphthylmethane dyes.
2001-08-15
Improvement of the synthesis of diphenylmethyl 7beta-(o-hydroxy)benzylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate.
2001-08
Costs and resources associated with the treatment of overactive bladder using retrospective medical care claims data.
2001-08
Successful treatment of excessive daytime sleepiness in Parkinson's disease with modafinil.
2001-07
Fatigue in multiple sclerosis.
2001-05
[Reducing of hepatotoxicity of antineoplastic chemotherapy and concomitant viral infection through control of liver metabolism: from experiment to clinical practice].
2001
Toxicology of environmental estrogens.
2001
Modafinil in fibromyalgia treatment.
2001
Antioxidant activity of 5-alkoxymethyl-6-chromanols.
2001
Safety profile of tolterodine as used in general practice in England: results of prescription-event monitoring.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:57:41 GMT 2025
Edited
by admin
on Mon Mar 31 18:57:41 GMT 2025
Record UNII
K3E387I0BC
Record Status Validated (UNII)
Record Version
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Name Type Language
DIPHENYL METHANE
INCI  
INCI  
Preferred Name English
Diphenylmethane
MI  
Systematic Name English
DITAN
Common Name English
BENZYLBENZENE
Systematic Name English
1,1'-METHYLENEBISBENZENE
HSDB  
Systematic Name English
1,1'-METHYLENEBISBENZENE [HSDB]
Common Name English
DIPHENYLMETHANE [MI]
Common Name English
NSC-4708
Code English
Code System Code Type Description
CAS
101-81-5
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
EVMPD
SUB182495
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
CHEBI
38884
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
PUBCHEM
7580
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
WIKIPEDIA
Diphenylmethane
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
MERCK INDEX
m4632
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
202-978-6
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
FDA UNII
K3E387I0BC
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
NSC
4708
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
HSDB
5141
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
SMS_ID
100000168908
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
MESH
C010129
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID1041891
Created by admin on Mon Mar 31 18:57:41 GMT 2025 , Edited by admin on Mon Mar 31 18:57:41 GMT 2025
PRIMARY
Related Record Type Details
METABOLITE -> PARENT
METABOLITE -> PARENT