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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H20ClN3O4
Molecular Weight 389.833
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLOPYRIMORATE

SMILES

CC1=C(OC2=NN=C(Cl)C=C2OC(=O)N3CCOCC3)C(=CC=C1)C4CC4

InChI

InChIKey=BXIGJZDQFDFASM-UHFFFAOYSA-N
InChI=1S/C19H20ClN3O4/c1-12-3-2-4-14(13-5-6-13)17(12)27-18-15(11-16(20)21-22-18)26-19(24)23-7-9-25-10-8-23/h2-4,11,13H,5-10H2,1H3

HIDE SMILES / InChI

Molecular Formula C19H20ClN3O4
Molecular Weight 389.833
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:59:32 GMT 2025
Edited
by admin
on Mon Mar 31 19:59:32 GMT 2025
Record UNII
0SVL4HSS2F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SW-065
Preferred Name English
CYCLOPYRIMORATE
ISO  
Common Name English
4-MORPHOLINECARBOXYLIC ACID, 6-CHLORO-3-(2-CYCLOPROPYL-6-METHYLPHENOXY)-4-PYRIDAZINYL ESTER
Systematic Name English
CYCLOPYRIMORATE [ISO]
Common Name English
Code System Code Type Description
PUBCHEM
23013854
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
PRIMARY
ALANWOOD
cyclopyrimorate
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
PRIMARY
CAS
1236401-29-8
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
SUPERSEDED
FDA UNII
0SVL4HSS2F
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
PRIMARY
CAS
499231-24-2
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID40198157
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
PRIMARY
CHEBI
142780
Created by admin on Mon Mar 31 19:59:32 GMT 2025 , Edited by admin on Mon Mar 31 19:59:32 GMT 2025
PRIMARY