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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H29N3O
Molecular Weight 339.4745
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DISOPYRAMIDE, (S)-

SMILES

CC(C)N(CC[C@](C(N)=O)(C1=CC=CC=C1)C2=CC=CC=N2)C(C)C

InChI

InChIKey=UVTNFZQICZKOEM-NRFANRHFSA-N
InChI=1S/C21H29N3O/c1-16(2)24(17(3)4)15-13-21(20(22)25,18-10-6-5-7-11-18)19-12-8-9-14-23-19/h5-12,14,16-17H,13,15H2,1-4H3,(H2,22,25)/t21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H29N3O
Molecular Weight 339.4745
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 Mon Mar 31 17:54:04 GMT 2025
Edited
by admin
on Mon Mar 31 17:54:04 GMT 2025
Record UNII
4HB8OU08NH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DISOPYRAMIDE, (S)-
Common Name English
(+)-(S)-DISOPYRAMIDE
Preferred Name English
D-DISOPYRAMIDE
Common Name English
2-PYRIDINEACETAMIDE, .ALPHA.-(2-(BIS(1-METHYLETHYL)AMINO)ETHYL)-.ALPHA.-PHENYL-, (.ALPHA.S)-
Systematic Name English
(S)-(+)-DISOPYRAMIDE
Common Name English
(S)-DISOPYRAMIDE
Common Name English
DISOPYRAMIDE, D-
Common Name English
(+)-DISOPYRAMIDE
Common Name English
2-PYRIDINEACETAMIDE, .ALPHA.-(2-(BIS(1-METHYLETHYL)AMINO)ETHYL)-.ALPHA.-PHENYL-, (S)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID301043597
Created by admin on Mon Mar 31 17:54:04 GMT 2025 , Edited by admin on Mon Mar 31 17:54:04 GMT 2025
PRIMARY
PUBCHEM
156295
Created by admin on Mon Mar 31 17:54:04 GMT 2025 , Edited by admin on Mon Mar 31 17:54:04 GMT 2025
PRIMARY
CAS
112346-85-7
Created by admin on Mon Mar 31 17:54:04 GMT 2025 , Edited by admin on Mon Mar 31 17:54:04 GMT 2025
SUPERSEDED
FDA UNII
4HB8OU08NH
Created by admin on Mon Mar 31 17:54:04 GMT 2025 , Edited by admin on Mon Mar 31 17:54:04 GMT 2025
PRIMARY
CAS
74464-84-9
Created by admin on Mon Mar 31 17:54:04 GMT 2025 , Edited by admin on Mon Mar 31 17:54:04 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER