Diethofencarb

Diethofencarb
Names
Preferred IUPAC name
propan-2-yl N-(3,4-diethoxyphenyl)carbamate
Other names
Diethofencarb
Identifiers
CAS Number
  • 87130-20-9
3D model (JSmol)
  • Interactive image
Beilstein Reference
 8393454
ChEBI
  • CHEBI:4520
ChEMBL
  • ChEMBL1880404
ChemSpider
  • 82840
ECHA InfoCard 100.118.674 Edit this at Wikidata
EC Number
  • 617-968-0
KEGG
  • C11077
PubChem CID
  • 91742
UNII
  • 421BLT77U4
CompTox Dashboard (EPA)
  • DTXSID5037527 Edit this at Wikidata
InChI
  • InChI=1S/C14H21NO4/c1-5-17-12-8-7-11(9-13(12)18-6-2)15-14(16)19-10(3)4/h7-10H,5-6H2,1-4H3,(H,15,16)
    Key: LNJNFVJKDJYTEU-UHFFFAOYSA-N
  • CCOC1=C(C=C(C=C1)NC(=O)OC(C)C)OCC
Properties
Chemical formula
 C14H21NO4
Molar mass 267.325 g·mol−1
Hazards
GHS labelling:[1]
Pictograms
 GHS07: Exclamation mark
Warning
Hazard statements
 H319
Precautionary statements
 P264+P265, P280, P305+P351+P338, P337+P317
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Diethofencarb is a carbamate fungicide which is used to control Botrytis infections on a variety of fruit and vegetable crops.[2][3]

References

  1. ^ "Diethofencarb". pubchem.ncbi.nlm.nih.gov.
  2. ^ Leroux P, Fritz R, Debieu D, Albertini C, Lanen C, Bach J, et al. (September 2002). "Mechanisms of resistance to fungicides in field strains of Botrytis cinerea". Pest Management Science. 58 (9): 876–888. doi:10.1002/ps.566. PMID 12233177.
  3. ^ Liu YH, Yuan SK, Hu XR, Zhang CQ (August 2019). "Shift of Sensitivity in Botrytis cinerea to Benzimidazole Fungicides in Strawberry Greenhouse Ascribing to the Rising-lowering of E198A Subpopulation and its Visual, On-site Monitoring by Loop-mediated Isothermal Amplification". Scientific Reports. 9 (1): 11644. Bibcode:2019NatSR...911644L. doi:10.1038/s41598-019-48264-4. PMC 6690993. PMID 31406191.


  • v
  • t
  • e