TRIBENURON-METHYL

Investigational

Details

Stereochemistry	ACHIRAL
Molecular Formula	C15H17N5O6S
Molecular Weight	395.39
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)N(C)C2=NC(OC)=NC(C)=N2

InChI

InChIKey=VLCQZHSMCYCDJL-UHFFFAOYSA-N

InChI=1S/C15H17N5O6S/c1-9-16-13(18-14(17-9)26-4)20(2)15(22)19-27(23,24)11-8-6-5-7-10(11)12(21)25-3/h5-8H,1-4H3,(H,19,22)

HIDE SMILES / InChI

Molecular Formula	C15H17N5O6S
Molecular Weight	395.39
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Mineralisation studies of 14C-labelled metsulfuron-methyl, tribenuron-methyl, chlorsulfuron and thifensulfuron-methyl in one Danish soil and groundwater sediment profile.	2001 Nov	11695596
Light-induced transformation of tribenuron-methyl on glass, soil, and plant surface.	2002 Mar	11990367
Common and distinct gene expression patterns induced by the herbicides 2,4-dichlorophenoxyacetic acid, cinidon-ethyl and tribenuron-methyl in wheat.	2006 Dec	17054088
No-tillage system applied to the sunflower (hybrid pioneer PR64E83) resistant to the tribenuron-methyl in the conditions from Romania.	2007	18399451
Chemical cotton stalk destruction for maintenance of host-free periods for the control of overwintering boll weevil in tropical and subtropical climates.	2007 Apr	17348066
Pesticides in surface drinking-water supplies of the northern Great Plains.	2007 Aug	17687445
Biodegradation of chlorimuron-ethyl by the bacterium Klebsiella jilinsis 2N3.	2010 Aug	20574870
Trace level determination of selected sulfonylurea herbicides in wetland sediment by liquid chromatography electrospray tandem mass spectrometry.	2010 Jan	20390926
Leaching of three sulfonylurea herbicides during sprinkler irrigation.	2010 Jan-Feb	20048324
A composite transcriptional signature differentiates responses towards closely related herbicides in Arabidopsis thaliana and Brassica napus.	2010 Mar	20043233
Sulfonylureas have antifungal activity and are potent inhibitors of Candida albicans acetohydroxyacid synthase.	2013 Jan 10	23237384

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:13:06 GMT 2023` Edited by `admin` on `Fri Dec 15 19:13:06 GMT 2023`
Record UNII	D0493A985P
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

TRIBENURON-METHYL

Common Name

English

TRIBENURON METHYL ESTER

Common Name

English

TRIBENURON-METHYL [HSDB]

Common Name

English

TRIBENURON METHYL

Common Name

English

DPX-L 5300

Code

English

BENZOIC ACID, 2-(((((4-METHOXY-6-METHYL-1,3,5-TRIAZIN-2- YL)METHYLAMINO)CARBONYL)AMINO)SULFONYL)-, METHYL ESTER

Common Name

English

TRIBENURON-METHYL [ISO]

Common Name

English

CAMEO (PESTICIDE)

Brand Name

English

GRANSTAR

Brand Name

English

QUANTUM

Brand Name

English

EXPRESS (PESTICIDE)

Brand Name

English

POINTER

Brand Name

English

HELM-TRIBI 75WG

Brand Name

English

HCHA 92HE

Brand Name

English

SULFMETHMETON-METHYL

Common Name

English

AGROSTAR

Brand Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

128887