U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H21N
Molecular Weight 155.2804
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOPROPYLHEXEDRINE

SMILES

CN[C@@H](C)CC1CCCCC1

InChI

InChIKey=JCRIVQIOJSSCQD-VIFPVBQESA-N
InChI=1S/C10H21N/c1-9(11-2)8-10-6-4-3-5-7-10/h9-11H,3-8H2,1-2H3/t9-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H21N
Molecular Weight 155.2804
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:06:06 UTC 2023
Edited
by admin
on Fri Dec 15 16:06:06 UTC 2023
Record UNII
4R3L4TYV09
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOPROPYLHEXEDRINE
INN   WHO-DD  
INN  
Official Name English
levopropylhexedrine [INN]
Common Name English
L-PROPYLHEXEDRINE
Common Name English
L-1-CYCLOHEXYL-2-METHYLAMINOPROPANE
Common Name English
Levopropylhexedrine [WHO-DD]
Common Name English
EVENTIN
Brand Name English
PROPYLHEXEDRINE L-FORM [MI]
Common Name English
(-)-N,.ALPHA.-DIMETHYLCYCLOHEXANEETHYLAMINE
Systematic Name English
PROPYLHEXEDRINE, (S)-
Common Name English
(-)-PROPYLHEXEDRINE
Common Name English
CYCLOHEXANEETHANAMINE, N,.ALPHA.-DIMETHYL-, (.ALPHA.S)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
Code System Code Type Description
WIKIPEDIA
Levopropylhexedrine
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
CAS
53690-40-7
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
SUPERSEDED
CAS
50453-50-4
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
SUPERSEDED
SMS_ID
100000082282
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
EPA CompTox
DTXSID801024267
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
NCI_THESAURUS
C83883
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
FDA UNII
4R3L4TYV09
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
MERCK INDEX
m9242
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2105014
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
ECHA (EC/EINECS)
228-245-0
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
CAS
42870-71-3
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
SUPERSEDED
EVMPD
SUB08487MIG
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
CAS
6192-97-8
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
INN
4279
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
PUBCHEM
71197
Created by admin on Fri Dec 15 16:06:06 UTC 2023 , Edited by admin on Fri Dec 15 16:06:06 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
RACEMATE -> ENANTIOMER
Related Record Type Details
ACTIVE MOIETY