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Details

Stereochemistry ACHIRAL
Molecular Formula C13H13N.ClH
Molecular Weight 219.71
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Benzhydrylamine hydrochloride

SMILES

Cl.NC(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=CIHWJRSPVJBHGT-UHFFFAOYSA-N
InChI=1S/C13H13N.ClH/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10,13H,14H2;1H

HIDE SMILES / InChI

Molecular Formula C13H13N
Molecular Weight 183.249
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Benzhydrylamine linker grafting: a strategy for the improved synthesis of C-terminal peptide amides.
2010-10
Synthesis and comparative properties of two amide-generating resin linkers for use in solid phase peptide synthesis.
2010-10
Preparation of honeycomb scaffold with hierarchical porous structures by core-crosslinked core-corona nanoparticles.
2009-04-01
Design and combinatorial synthesis of a library of methylenesulfonamides and related compounds as potential kinase inhibitors.
2009-03
Palladium-catalyzed benzylic arylation of N-benzylxanthone imine.
2008-10-16
4-(4-Bromo-benzyl-ideneamino)-1-(diphenyl-amino-meth-yl)-3-[1-(4-isobutyl-phen-yl)eth-yl]-1H-1,2,4-triazole-5(4H)-thione.
2008-05-07
VivaGel (SPL7013 Gel): a candidate dendrimer--microbicide for the prevention of HIV and HSV infection.
2007
N-8-Substituted benztropinamine analogs as selective dopamine transporter ligands.
2005-12-15
Synthesis, further biological evaluation and pharmacodynamics of newly discovered inhibitors of TNF-alpha production.
2003-09-01
Physicochemical and chromatographic evaluation of benzhydrylamine-resin as an anion exchanger solid support.
2003-07-31
Novel 4-alkyl-1-arylpiperazines and 1,2,3,4-tetrahydroisoquinolines containing diphenylmethylamino or diphenylmethoxy fragment with differentiated 5-HT1A/5-HT2A/D2 receptor activity.
2003-05-26
Neuroprotective and cognition-enhancing properties of MK-801 flexible analogs. Structure-activity relationships.
2001-06
Patents
Substance Class Chemical
Created
by admin
on Tue Apr 01 17:15:53 GMT 2025
Edited
by admin
on Tue Apr 01 17:15:53 GMT 2025
Record UNII
LZ568SDT78
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Benzhydrylammonium chloride
Preferred Name English
Benzhydrylamine hydrochloride
Systematic Name English
Benzenemethanamine, ?-phenyl-, hydrochloride (1:1)
Systematic Name English
1,1-Diphenylmethylamine hydrochloride
Systematic Name English
NSC-18792
Code English
Code System Code Type Description
PUBCHEM
78921
Created by admin on Tue Apr 01 17:15:53 GMT 2025 , Edited by admin on Tue Apr 01 17:15:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID00200644
Created by admin on Tue Apr 01 17:15:53 GMT 2025 , Edited by admin on Tue Apr 01 17:15:53 GMT 2025
PRIMARY
NSC
18792
Created by admin on Tue Apr 01 17:15:53 GMT 2025 , Edited by admin on Tue Apr 01 17:15:53 GMT 2025
PRIMARY
FDA UNII
LZ568SDT78
Created by admin on Tue Apr 01 17:15:53 GMT 2025 , Edited by admin on Tue Apr 01 17:15:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
226-084-0
Created by admin on Tue Apr 01 17:15:53 GMT 2025 , Edited by admin on Tue Apr 01 17:15:53 GMT 2025
PRIMARY
CAS
5267-34-5
Created by admin on Tue Apr 01 17:15:53 GMT 2025 , Edited by admin on Tue Apr 01 17:15:53 GMT 2025
PRIMARY