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Details

Stereochemistry RACEMIC
Molecular Formula C12H18ClN.ClH
Molecular Weight 248.192
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEFENOREX HYDROCHLORIDE

SMILES

Cl.CC(CC1=CC=CC=C1)NCCCCl

InChI

InChIKey=IDHNGYVCZUQHFV-UHFFFAOYSA-N
InChI=1S/C12H18ClN.ClH/c1-11(14-9-5-8-13)10-12-6-3-2-4-7-12;/h2-4,6-7,11,14H,5,8-10H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula C12H18ClN
Molecular Weight 211.731
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 15:28:56 UTC 2023
Edited
by admin
on Fri Dec 15 15:28:56 UTC 2023
Record UNII
6X1N18AU15
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEFENOREX HYDROCHLORIDE
MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
RO-4-5282
Code English
Mefenorex hydrochloride [WHO-DD]
Common Name English
N-(3-Chloropropyl)-α-methylphenethylamine hydrochloride
Systematic Name English
MEFENOREX HYDROCHLORIDE [MART.]
Common Name English
MEFENOREX HYDROCHLORIDE [MI]
Common Name English
(±)-MEFENOREX HYDROCHLORIDE
Common Name English
MEFENOREX HYDROCHLORIDE [USAN]
Common Name English
RO 4-5282
Code English
NSC-133749
Code English
MEFENOREX HYDROCHLORIDE, (±)-
Common Name English
MEFENOREX HCL
Common Name English
MEFENOREX HYDROCHLDRIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29728
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
Code System Code Type Description
PUBCHEM
21776
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
SMS_ID
100000086166
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110962
Created by admin on Fri Dec 15 15:28:56 UTC 2023 , Edited by admin on Fri Dec 15 15:28:56 UTC 2023
PRIMARY
ECHA (EC/EINECS)
226-985-9
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
MERCK INDEX
m7140
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY Merck Index
MESH
C000450
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
EVMPD
SUB03115MIG
Created by admin on Fri Dec 15 15:28:56 UTC 2023 , Edited by admin on Fri Dec 15 15:28:56 UTC 2023
PRIMARY
NSC
133749
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
FDA UNII
6X1N18AU15
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
NCI_THESAURUS
C77848
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY
CAS
5586-87-8
Created by admin on Fri Dec 15 15:28:56 UTC 2023 , Edited by admin on Fri Dec 15 15:28:56 UTC 2023
PRIMARY
RXCUI
236179
Created by admin on Fri Dec 15 15:28:57 UTC 2023 , Edited by admin on Fri Dec 15 15:28:57 UTC 2023
PRIMARY RxNorm
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY