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Diethofencarb

From Wikipedia, the free encyclopedia

Diethofencarb
Names
Preferred IUPAC name
propan-2-yl N-(3,4-diethoxyphenyl)carbamate
Other names
Diethofencarb
Identifiers
3D model (JSmol)
8393454
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.118.674 Edit this at Wikidata
EC Number
  • 617-968-0
KEGG
UNII
  • 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
C14H21NO4
Molar mass 267.325 g·mol−1
Hazards
GHS labelling:[1]
GHS07: Exclamation mark
Warning
H319
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).

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.


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This page was last edited on 27 February 2024, at 19:12
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