LACTOFEN

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H15ClF3NO7
Molecular Weight	461.773
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCOC(=O)C(C)OC(=O)C1=CC(OC2=CC=C(C=C2Cl)C(F)(F)F)=CC=C1[N+]([O-])=O

InChI

InChIKey=CONWAEURSVPLRM-UHFFFAOYSA-N

InChI=1S/C19H15ClF3NO7/c1-3-29-17(25)10(2)30-18(26)13-9-12(5-6-15(13)24(27)28)31-16-7-4-11(8-14(16)20)19(21,22)23/h4-10H,3H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C19H15ClF3NO7
Molecular Weight	461.773
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

PubMed

Title	Date	PubMed
Environmental impact on vascular development predicted by high-throughput screening.	2011-11	21788198
Biotransformation of the diphenyl ether herbicide lactofen and purification of a lactofen esterase from Brevundimonas sp. LY-2.	2010-09-08	20712347
In vitro screening of environmental chemicals for targeted testing prioritization: the ToxCast project.	2010-04	20368123
Impact of environmental chemicals on key transcription regulators and correlation to toxicity end points within EPA's ToxCast program.	2010-03-15	20143881
Enantioselective degradation in sediment and aquatic toxicity to Daphnia magna of the herbicide lactofen enantiomers.	2010-02-24	20088506
Biodegradation of fomesafen by strain Lysinibacillus sp. ZB-1 isolated from soil.	2009-12	19846192
Influence of soil properties on the enantioselective dissipation of the herbicide lactofen in soils.	2009-07-08	19507858
The chiral resolution of pesticides on amylose-tris(3,5-dimethylphenylcarbamate) CSP by HPLC and the enantiomeric identification by circular dichroism.	2008-01	17957825
PPARalpha- and DEHP-Induced Cancers.	2008	18769559
Soil amendment: a technique for soil remediation of lactofen.	2007-07	17599224
Enantiomeric separation of chiral pesticides by high performance liquid chromatography on cellulose tris-3,5-dimethyl carbamate stationary phase under reversed phase conditions.	2007-02	17396588
Chiral separations of pesticide enantiomers by high-performance liquid chromatography using cellulose triphenylcarbamate chiral stationary phase.	2007-01-27	17254369
Determination of diphenylether herbicides in water samples by solid-phase microextraction coupled to liquid chromatography.	2006-11	17313105
Herbicide effects on cuticle ultrastructure in Eleusine indica and Portulaca oleracea.	2006-04	16845829
Enantiomeric resolution of chiral pesticides by high-performance liquid chromatography.	2006-03-08	16506803
The diphenylether herbicide lactofen induces cell death and expression of defense-related genes in soybean.	2005-12	16299178
Effects of pesticides on yeasts isolated from agricultural soil.	2004-01-10	14713165
Lactofen induces isoflavone accumulation and glyceollin elicitation competency in soybean.	2003-03	12590114
Induction of hepatic peroxisome proliferation in mice by lactofen, a diphenyl ether herbicide.	1988-03-30	3354002

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:27:57 GMT 2025` Edited by `admin` on `Mon Mar 31 22:27:57 GMT 2025`
Record UNII	L44N8UV47O
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

1'-(CARBOETHOXY)ETHYL 5-(2-CHLORO-4- (TRIFLUOROMETHYL)PHENOXY)-2-NITROBENZOATE

Preferred Name

English

LACTOFEN

Common Name

English

5-(2-CHLORO-4-(TRIFLUOROMETHYL)PHENOXY)-2-NITROBENZOIC ACID 2-ETHOXY-1-METHYL-2-OXOETHYL ESTER

Systematic Name

English

PHOENIX (HERBICIDE)

Common Name

English

COBRA HERBICIDE [HSDB]

Common Name

English

BENZOIC ACID, 5-(2-CHLORO-4-(TRIFLUOROMETHYL)PHENOXY)-2- NITRO-, 2-ETHOXY-1-METHYL-2-OXOETHYL ESTER

Common Name

English

2-ETHOXY-1-METHYL-2-OXOETHYL 5-(2-CHLORO-4- (TRIFLUOROMETHYL)PHENOXY)-2 NITROBENZOATE, (±)-

Systematic Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

128888