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Details

Stereochemistry ACHIRAL
Molecular Formula C12H16ClN3O.ClH
Molecular Weight 290.189
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBANTEL HYDROCHLORIDE

SMILES

Cl.CCCCC(=N)NC(=O)NC1=CC=C(Cl)C=C1

InChI

InChIKey=QVZNPPSDXAGRRO-UHFFFAOYSA-N
InChI=1S/C12H16ClN3O.ClH/c1-2-3-4-11(14)16-12(17)15-10-7-5-9(13)6-8-10;/h5-8H,2-4H2,1H3,(H3,14,15,16,17);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 C12H16ClN3O
Molecular Weight 253.728
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

PubMed

PubMed

TitleDatePubMed
Imidoylureas. A new class of anthelmintics.
1969-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:48:33 GMT 2025
Edited
by admin
on Mon Mar 31 17:48:33 GMT 2025
Record UNII
W6LI9H8249
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PENTANIMIDAMIDE, N-(((4-CHLOROPHENYL)AMINO)CARBONYL)-, HYDROCHLORIDE (1:1)
Preferred Name English
CARBANTEL HYDROCHLORIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Mon Mar 31 17:48:33 GMT 2025 , Edited by admin on Mon Mar 31 17:48:33 GMT 2025
Code System Code Type Description
FDA UNII
W6LI9H8249
Created by admin on Mon Mar 31 17:48:33 GMT 2025 , Edited by admin on Mon Mar 31 17:48:33 GMT 2025
PRIMARY
NCI_THESAURUS
C96556
Created by admin on Mon Mar 31 17:48:33 GMT 2025 , Edited by admin on Mon Mar 31 17:48:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID10179776
Created by admin on Mon Mar 31 17:48:33 GMT 2025 , Edited by admin on Mon Mar 31 17:48:33 GMT 2025
PRIMARY
PUBCHEM
21508097
Created by admin on Mon Mar 31 17:48:33 GMT 2025 , Edited by admin on Mon Mar 31 17:48:33 GMT 2025
PRIMARY
CAS
25082-83-1
Created by admin on Mon Mar 31 17:48:33 GMT 2025 , Edited by admin on Mon Mar 31 17:48:33 GMT 2025
PRIMARY
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ACTIVE MOIETY