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

Details

Stereochemistry ABSOLUTE
Molecular Formula C13H26N2O
Molecular Weight 226.3583
Optical Activity ( - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Dihydrocuscohygrine, (-)-

SMILES

CN1CCC[C@H]1CC(O)C[C@@H]2CCCN2C

InChI

InChIKey=UOJNOOLFFFFKNA-RYUDHWBXSA-N
InChI=1S/C13H26N2O/c1-14-7-3-5-11(14)9-13(16)10-12-6-4-8-15(12)2/h11-13,16H,3-10H2,1-2H3/t11-,12-/m0/s1

HIDE SMILES / InChI

Molecular Formula C13H26N2O
Molecular Weight 226.3583
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 10:31:20 GMT 2025
Edited
by admin
on Wed Apr 02 10:31:20 GMT 2025
Record UNII
S8NA96NN7T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(-)-Dihydrocuscohygrine
Preferred Name English
Dihydrocuscohygrine, (-)-
Common Name English
CUSCOHYGRINOL
Systematic Name English
DIHYDROCUSCOHYGRINE
Common Name English
1,3-bis((S)-1-methylpyrrolidin-2-yl)propan-2-ol
Systematic Name English
(2S)-1-METHYL-.ALPHA.-(((2S)-1-METHYL-2-PYRROLIDINYL)METHYL)-2-PYRROLIDINEETHANOL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID901045577
Created by admin on Wed Apr 02 10:31:20 GMT 2025 , Edited by admin on Wed Apr 02 10:31:20 GMT 2025
PRIMARY
FDA UNII
S8NA96NN7T
Created by admin on Wed Apr 02 10:31:20 GMT 2025 , Edited by admin on Wed Apr 02 10:31:20 GMT 2025
PRIMARY
PUBCHEM
11075129
Created by admin on Wed Apr 02 10:31:20 GMT 2025 , Edited by admin on Wed Apr 02 10:31:20 GMT 2025
PRIMARY
WIKIPEDIA
Dihydrocuscohygrine
Created by admin on Wed Apr 02 10:31:20 GMT 2025 , Edited by admin on Wed Apr 02 10:31:20 GMT 2025
PRIMARY
CAS
58131-40-1
Created by admin on Wed Apr 02 10:31:20 GMT 2025 , Edited by admin on Wed Apr 02 10:31:20 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
ENANTIOMER -> ENANTIOMER