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Details

Stereochemistry ACHIRAL
Molecular Formula C7H4ClNO2
Molecular Weight 169.565
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-CHLORO-2,3-DIHYDROBENZOXAZOL-2-ONE

SMILES

ClC1=CC2=C(NC(=O)O2)C=C1

InChI

InChIKey=MATCZHXABVLZIE-UHFFFAOYSA-N
InChI=1S/C7H4ClNO2/c8-4-1-2-5-6(3-4)11-7(10)9-5/h1-3H,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C7H4ClNO2
Molecular Weight 169.565
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Enantioselective environmental behavior of the chiral herbicide fenoxaprop-ethyl and its chiral metabolite fenoxaprop in soil.
2010-12-22
Evolution of toxicity upon hydrolysis of fenoxaprop-p-ethyl.
2007-09-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:42:39 GMT 2025
Edited
by admin
on Mon Mar 31 22:42:39 GMT 2025
Record UNII
PG1JLE50LE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6-CHLORO-2,3-DIHYDROBENZOXAZOL-2-ONE
Systematic Name English
NSC-26191
Preferred Name English
6-CHLORO-2-BENZOXAZOLINONE
Systematic Name English
6-CHLOROBENZOXAZOLONE
Systematic Name English
2(3H)-BENZOXAZOLONE, 6-CHLORO-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 629092
Created by admin on Mon Mar 31 22:42:39 GMT 2025 , Edited by admin on Mon Mar 31 22:42:39 GMT 2025
Code System Code Type Description
FDA UNII
PG1JLE50LE
Created by admin on Mon Mar 31 22:42:39 GMT 2025 , Edited by admin on Mon Mar 31 22:42:39 GMT 2025
PRIMARY
CAS
19932-84-4
Created by admin on Mon Mar 31 22:42:39 GMT 2025 , Edited by admin on Mon Mar 31 22:42:39 GMT 2025
PRIMARY
NSC
26191
Created by admin on Mon Mar 31 22:42:39 GMT 2025 , Edited by admin on Mon Mar 31 22:42:39 GMT 2025
PRIMARY
PUBCHEM
29858
Created by admin on Mon Mar 31 22:42:39 GMT 2025 , Edited by admin on Mon Mar 31 22:42:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID2041545
Created by admin on Mon Mar 31 22:42:39 GMT 2025 , Edited by admin on Mon Mar 31 22:42:39 GMT 2025
PRIMARY