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Details

Stereochemistry RACEMIC
Molecular Formula C18H21NO.ClH
Molecular Weight 303.826
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIPRADROL HYDROCHLORIDE

SMILES

Cl.OC(C1CCCCN1)(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=KIFIYUHFHGSNHL-UHFFFAOYSA-N
InChI=1S/C18H21NO.ClH/c20-18(15-9-3-1-4-10-15,16-11-5-2-6-12-16)17-13-7-8-14-19-17;/h1-6,9-12,17,19-20H,7-8,13-14H2;1H

HIDE SMILES / InChI

Molecular Formula C18H21NO
Molecular Weight 267.3654
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:56:11 UTC 2023
Edited
by admin
on Fri Dec 15 16:56:11 UTC 2023
Record UNII
F6E46VR9Y2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIPRADROL HYDROCHLORIDE
JAN   MART.   MI   WHO-DD  
Common Name English
MERATONIC
Common Name English
PIPRADOLE HYDROCHLORIDE
Common Name English
2-PIPERIDINEMETHANOL, .ALPHA.,.ALPHA.-DIPHENYL-, HYDROCHLORIDE
Systematic Name English
PIPRADROL HYDROCHLORIDE [JAN]
Common Name English
MERATRAN HYDROCHLORIDE
Common Name English
PIPRADROL HCL
Common Name English
PIPRADROL HYDROCHLORIDE [MI]
Common Name English
MERATRANS
Common Name English
.ALPHA.,.ALPHA.-DIPHENYL-2-PIPERIDINEMETHANOL HYDROCHLORIDE
Systematic Name English
LEPTIDROL
Brand Name English
PIPRAL
Common Name English
GERODIL
Common Name English
STIMOLAG FORTIS
Common Name English
DETARIL
Brand Name English
Pipradrol hydrochloride [WHO-DD]
Common Name English
MERATRAN
Brand Name English
LUXIDIN
Brand Name English
PIPRADROL HYDROCHLORIDE [MART.]
Common Name English
2-PIPERIDINEMETHANOL, .ALPHA.,.ALPHA.-DIPHENYL-, HYDROCHLORIDE (1:1)
Systematic Name English
PIPERADROL HYDROCHLORIDE
Common Name English
Code System Code Type Description
MERCK INDEX
m8867
Created by admin on Fri Dec 15 16:56:12 UTC 2023 , Edited by admin on Fri Dec 15 16:56:12 UTC 2023
PRIMARY Merck Index
FDA UNII
F6E46VR9Y2
Created by admin on Fri Dec 15 16:56:12 UTC 2023 , Edited by admin on Fri Dec 15 16:56:12 UTC 2023
PRIMARY
EVMPD
SUB03864MIG
Created by admin on Fri Dec 15 16:56:11 UTC 2023 , Edited by admin on Fri Dec 15 16:56:11 UTC 2023
PRIMARY
SMS_ID
100000085310
Created by admin on Fri Dec 15 16:56:12 UTC 2023 , Edited by admin on Fri Dec 15 16:56:12 UTC 2023
PRIMARY
PUBCHEM
66008
Created by admin on Fri Dec 15 16:56:12 UTC 2023 , Edited by admin on Fri Dec 15 16:56:12 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110938
Created by admin on Fri Dec 15 16:56:11 UTC 2023 , Edited by admin on Fri Dec 15 16:56:11 UTC 2023
PRIMARY
CAS
71-78-3
Created by admin on Fri Dec 15 16:56:11 UTC 2023 , Edited by admin on Fri Dec 15 16:56:11 UTC 2023
PRIMARY
EPA CompTox
DTXSID50991292
Created by admin on Fri Dec 15 16:56:12 UTC 2023 , Edited by admin on Fri Dec 15 16:56:12 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-764-7
Created by admin on Fri Dec 15 16:56:12 UTC 2023 , Edited by admin on Fri Dec 15 16:56:12 UTC 2023
PRIMARY
DRUG BANK
DBSALT001777
Created by admin on Fri Dec 15 16:56:11 UTC 2023 , Edited by admin on Fri Dec 15 16:56:11 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY