Basic Description

Synonyms	methyl (2E)-2-methoxyimino-2-[2-[[(Z)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate \| methyl (2E)-(methoxyimino)[2-({[(E)-{1-[3-(trifluoromethyl)phenyl]ethylidene}amino]oxy}methyl)phenyl]acetate \| NCGC00163847-01 \| Benzeneacetic ac
Specifications & Purity	analytical standard
Shipped In	Normal
Grade	analytical standard
Product Description	Trifloxystrobin is a broad spectrum fungicide that inhibits fungal spore germination. A strobilurin class fungicide.

Associated Targets(Human)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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VDR Tclin Vitamin D receptor (26531 Activities)

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PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

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RXRA Tclin Retinoid X receptor alpha (3637 Activities)

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AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

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Associated Targets(non-human)

Cercospora beticola (433 Activities)

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Blumeria graminis (462 Activities)

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Botrytis cinerea (4183 Activities)

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Colletotrichum lagenaria (239 Activities)

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Pyricularia oryzae (1832 Activities)

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Solanum lycopersicum (493 Activities)

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Fulvia fulva (138 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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Verticillium dahliae (119 Activities)

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Solanum melongena (11 Activities)

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Erysiphe necator (54 Activities)

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Pseudoperonospora cubensis (1623 Activities)

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Pseudopyrenochaeta lycopersici (6 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	methyl (2E)-2-methoxyimino-2-[2-[[(E)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate
INCHI	InChI=1S/C20H19F3N2O4/c1-13(14-8-6-9-16(11-14)20(21,22)23)24-29-12-15-7-4-5-10-17(15)18(25-28-3)19(26)27-2/h4-11H,12H2,1-3H3/b24-13+,25-18+
InChi Key	ONCZDRURRATYFI-TVJDWZFNSA-N
Canonical SMILES	CC(=NOCC1=CC=CC=C1C(=NOC)C(=O)OC)C2=CC(=CC=C2)C(F)(F)F
Isomeric SMILES	C/C(=N\OCC1=CC=CC=C1/C(=N\OC)/C(=O)OC)/C2=CC(=CC=C2)C(F)(F)F
WGK Germany	2
PubChem CID	11664966
Molecular Weight	408.37

Certificates

Certificate of Analysis(COA)

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1 results found

Lot Number	Certificate Type	Date	Item
A2009120	Certificate of Analysis	Oct 07, 2023	T129128

Chemical and Physical Properties

Flash Point(°F)	70 °C
Flash Point(°C)	70°C
Boil Point(°C)	312 °C
Melt Point(°C)	72.9°C

Safety and Hazards(GHS)

WGK Germany	2

FAQs and Articles

FAQ

Trifluoromethyl in organic synthesis

Categories: Technical articles

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Sorafenib tosylate Fluoxetine Trifloxystrobin Fluorine block

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Wenhui Li, Ying Gu, Zikun Liu, Rimao Hua, Xiangwei Wu, Jiaying Xue. (2022) Development of a polyurethane-coated thin film solid phase microextraction device for multi-residue monitoring of pesticides in fruit and tea beverages. JOURNAL OF SEPARATION SCIENCE, 46 (2): (2200661). [PMID:36373185]
2. Kun Jia, Guilan Chen, Junquan Zeng, Fasheng Liu, Xinjun Liao, Chen Guo, Jiaqi Luo, Guanghua Xiong, Huiqiang Lu. (2022) Low trifloxystrobin-tebuconazole concentrations induce cardiac and developmental toxicity in zebrafish by regulating notch mediated‐oxidative stress generation. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 241 (113752). [PMID:35709675]
3. Qian Wang, Yujie Wu, Wei Guo, Feifang Zhang, Feng Zhang. (2022) A magnetic covalent organic framework as selective adsorbent for preconcentration of multi strobilurin fungicides in foods. FOOD CHEMISTRY, 392 (133190). [PMID:35636183]
4. Xiao Y. Li, Ying J. Qin, Yue Wang, Tao Huang, Yuan H. Zhao, Xiao H. Wang, Christopher J. Martyniuk, Bing Yan. (2021) Relative comparison of strobilurin fungicides at environmental levels: Focus on mitochondrial function and larval activity in early staged zebrafish (Danio rerio). TOXICOLOGY, 452 (152706). [PMID:33548355]

References

1. Wenhui Li, Ying Gu, Zikun Liu, Rimao Hua, Xiangwei Wu, Jiaying Xue. (2022) Development of a polyurethane-coated thin film solid phase microextraction device for multi-residue monitoring of pesticides in fruit and tea beverages. JOURNAL OF SEPARATION SCIENCE, 46 (2): (2200661). [PMID:36373185]
2. Kun Jia, Guilan Chen, Junquan Zeng, Fasheng Liu, Xinjun Liao, Chen Guo, Jiaqi Luo, Guanghua Xiong, Huiqiang Lu. (2022) Low trifloxystrobin-tebuconazole concentrations induce cardiac and developmental toxicity in zebrafish by regulating notch mediated‐oxidative stress generation. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 241 (113752). [PMID:35709675]
3. Qian Wang, Yujie Wu, Wei Guo, Feifang Zhang, Feng Zhang. (2022) A magnetic covalent organic framework as selective adsorbent for preconcentration of multi strobilurin fungicides in foods. FOOD CHEMISTRY, 392 (133190). [PMID:35636183]
4. Xiao Y. Li, Ying J. Qin, Yue Wang, Tao Huang, Yuan H. Zhao, Xiao H. Wang, Christopher J. Martyniuk, Bing Yan. (2021) Relative comparison of strobilurin fungicides at environmental levels: Focus on mitochondrial function and larval activity in early staged zebrafish (Danio rerio). TOXICOLOGY, 452 (152706). [PMID:33548355]

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Trifloxystrobin - analytical standard, high purity , CAS No.141517-21-7

Basic Description

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Certificates

Certificate of Analysis(COA)

Chemical and Physical Properties

Safety and Hazards(GHS)

Related Documents

FAQs and Articles

Citations of This Product

References

Solution Calculators

Molarity Calculator

Dilution Calculator

Reconstitution Calculator