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Details

Stereochemistry RACEMIC
Molecular Formula C10H16N2S.ClH
Molecular Weight 232.773
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MANOZODIL HYDROCHLORIDE

SMILES

Cl.CNCC1CCC2=C(C1)N=C(C)S2

InChI

InChIKey=GWYBXYYUSIJGTI-UHFFFAOYSA-N
InChI=1S/C10H16N2S.ClH/c1-7-12-9-5-8(6-11-2)3-4-10(9)13-7;/h8,11H,3-6H2,1-2H3;1H

HIDE SMILES / InChI

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

Molecular Formula C10H16N2S
Molecular Weight 196.312
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Manozodil is a vasodilator agent.

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:21:08 GMT 2025
Edited
by admin
on Mon Mar 31 23:21:08 GMT 2025
Record UNII
5Q34P8QF48
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-BENZOTHIAZOLEMETHANAMINE, 4,5,6,7-TETRAHYDRO-N,2-DIMETHYL-, HYDROCHLORIDE (1:1)
Preferred Name English
MANOZODIL HYDROCHLORIDE
Common Name English
5-BENZOTHIAZOLEMETHANAMINE, 4,5,6,7-TETRAHYDRO-N,2-DIMETHYL-, MONOHYDROCHLORIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID00998731
Created by admin on Mon Mar 31 23:21:08 GMT 2025 , Edited by admin on Mon Mar 31 23:21:08 GMT 2025
PRIMARY
FDA UNII
5Q34P8QF48
Created by admin on Mon Mar 31 23:21:08 GMT 2025 , Edited by admin on Mon Mar 31 23:21:08 GMT 2025
PRIMARY
CAS
95203-42-2
Created by admin on Mon Mar 31 23:21:08 GMT 2025 , Edited by admin on Mon Mar 31 23:21:08 GMT 2025
PRIMARY
CAS
77528-68-8
Created by admin on Mon Mar 31 23:21:08 GMT 2025 , Edited by admin on Mon Mar 31 23:21:08 GMT 2025
NON-SPECIFIC STOICHIOMETRY
ECHA (EC/EINECS)
278-714-9
Created by admin on Mon Mar 31 23:21:08 GMT 2025 , Edited by admin on Mon Mar 31 23:21:08 GMT 2025
PRIMARY
PUBCHEM
198580
Created by admin on Mon Mar 31 23:21:08 GMT 2025 , Edited by admin on Mon Mar 31 23:21:08 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY