Monolinuron - CAS 1746-81-2

Catalog:	BB059015
Product Name:	Monolinuron
CAS:	1746-81-2
Synonyms:	3-(4-Chlorophenyl)-1-methoxy-1-methylurea; Monorotox; Arezin; Premalin; Aresin; N'-(4-Chlorophenyl)-N-methoxy-N-methylurea

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Computed Properties

IUPAC Name:	3-(4-chlorophenyl)-1-methoxy-1-methylurea
Molecular Weight:	214.65
Molecular Formula:	C9H11ClN2O2
Canonical SMILES:	CN(C(=O)NC1=CC=C(C=C1)Cl)OC
InChI:	InChI=1S/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)
InChI Key:	LKJPSUCKSLORMF-UHFFFAOYSA-N
Melting Point:	80-83 °C
Solubility:	Sol in alcohol, Acetone, Benzene, Toluene
Appearance:	Colorless crystals
Stability:	Stable at melting point & in soln but slowly decomposes in acids & bases

Publication Number	Title	Priority Date
CN-114050874-A	Modulation calibration circuit and method	20220112
JP-2022031355-A	Pest control method	20211215
CN-114138669-A	Software automatic testing method based on function level selection symbolized mixed execution	20211210
CN-113895636-A	Embedded type invisible air inlet channel	20211118
CN-114158553-A	Novel pesticide preparation and preparation method thereof	20211110
JP-2022006186-A	Plant disease control method	20211028
JP-2022023190-A	Plant disease control method using methyltetraprowl	20211028
JP-2022001607-A	Plant disease control method using phenylpyrazole compound and phenyl compound	20211015
CN-113783393-A	Direct-current brushless motor, motor control system, rail train and control method	20211011
CN-215934689-U	Direct current brushless motor, motor control system and rail train	20211011

PMID	Publication Date	Title	Journal
22578198	20120530	Assessment of the leaching potential of 12 substituted phenylurea herbicides in two agricultural soils under laboratory conditions	Journal of agricultural and food chemistry
22590019	20120401	4-Chloro-anilinium 3-carb-oxy-prop-2-enoate	Acta crystallographica. Section E, Structure reports online
21482475	20110901	Sonochemical and sonocatalytic degradation of monolinuron in water	Ultrasonics sonochemistry
21287284	20110701	Investigation of photodegradation and hydrolysis of selected substituted urea and organophosphate pesticides in water	Environmental science and pollution research international
21626693	20110701	Ultrasonic nebulization extraction coupled with headspace hollow fiber microextraction of pesticides from root of Panax ginseng C.A. Mey	Journal of separation science
21110068	20110601	Isolation and characterization of an isoproturon mineralizing Sphingomonas sp. strain SH from a French agricultural soil	Biodegradation
21238727	20110215	Solvent (ionic liquid) impregnated resin-based extraction coupled with dynamic ultrasonic desorption for separation and concentration of four herbicides in environmental water	Talanta
22174632	20110101	Green aspects of techniques for the determination of currently used pesticides in environmental samples	International journal of molecular sciences
20401520	20101101	Efficient biotransformation of herbicide diuron by bacterial strain Micrococcus sp. PS-1	Biodegradation
20801343	20100915	Determination of phenylurea and triazine herbicides in milk by microwave assisted ionic liquid microextraction high-performance liquid chromatography	Talanta

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GHS Hazard Statement:	H302: Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P260, P264, P270, P273, P301+P317, P319, P330, P391, and P501
Signal Word:	Warning

Complexity:	193
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	214.0509053
Formal Charge:	0
Heavy Atom Count:	14
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	214.0509053
Rotatable Bond Count:	2
Topological Polar Surface Area:	41.6Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	2.3