Methazole: Difference between revisions

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			{{chembox
	'''Methazole''' (C<sub>9</sub>H<sub>6</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>3</sub>) is a ].
			\| Verifiedfields = changed
	==Names==
			\| Watchedfields = changed
	*Oxydiazol
			\| verifiedrevid = 432143455
	*VCS 438
			\| ImageFile = Methazole.png
	*Paxilon
			\| ImageSize = 200
	*Probe
			\| ImageAlt = Skeletal formula of methazole
			\| ImageFile1 = Methazole-3D-spacefill.png
			\| ImageSize1 = 200
			\| ImageAlt1 = Space-filling model of methazole
			\| PIN = 2-(3,4-Dichlorophenyl)-4-methyl-1,2,4-oxadiazolidine-3,5-dione
			\| OtherNames = Metazole; Oxydiazol; VCS 438; Paxilon; Probe; Metazol; Mezopur; Oxydiazol; Bioxone; Chlormethazole
			\|Section1={{Chembox Identifiers
			\| CASNo_Ref = {{cascite\|correct\|??}}
			\| CASNo = 20354-26-1
			\| UNII_Ref = {{fdacite\|changed\|FDA}}
			\| UNII = E35M7EMD3V
			\| PubChem = 4690
			\| KEGG_Ref = {{keggcite\|correct\|kegg}}
			\| KEGG = C19123
			\| SMILES = CN1C(=O)N(OC1=O)C2=CC(=C(C=C2)Cl)Cl
			\| ChemSpiderID_Ref = {{chemspidercite\|changed\|chemspider}}
			\| ChemSpiderID = 4528
			\| InChI = 1/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3
			\| InChIKey = LRUUNMYPIBZBQH-UHFFFAOYAP
			\| StdInChI_Ref = {{stdinchicite\|changed\|chemspider}}
			\| StdInChI = 1S/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3
			\| StdInChIKey_Ref = {{stdinchicite\|changed\|chemspider}}
			\| StdInChIKey = LRUUNMYPIBZBQH-UHFFFAOYSA-N
			}}
			\|Section2={{Chembox Properties
			\| C=9\|H=6\|Cl=2\|N=2\|O=3
			\| Appearance =
			\| Density =
			\| MeltingPt =
			\| BoilingPt =
			\| Solubility =
			}}
			\|Section3={{Chembox Hazards
			\| MainHazards =
			\| FlashPt =
			\| AutoignitionPt =
			}}
			}}

			'''Methazole''' (C<sub>9</sub>H<sub>6</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>3</sub>) is an obsolete<ref name=Hertfordshire>{{cite web \| url = https://sitem.herts.ac.uk/aeru/iupac/Reports/454.htm \| title = Methazole \| publisher = University of Hertfordshire}}</ref> ] in the family of herbicides known as ]s. It was used as a post-emergent treatment for controlling weeds.<ref name=Hertfordshire/>

			==References==
			{{reflist}}

			{{Herbicides}}
	{{organic-compound-stub}}

	]		]
			]
			]


			{{heterocyclic-stub}}

Latest revision as of 11:50, 17 March 2021

Methazole
Names


Preferred IUPAC name 2-(3,4-Dichlorophenyl)-4-methyl-1,2,4-oxadiazolidine-3,5-dione
Other names Metazole; Oxydiazol; VCS 438; Paxilon; Probe; Metazol; Mezopur; Oxydiazol; Bioxone; Chlormethazole
Identifiers
CAS Number	20354-26-1
3D model (JSmol)	Interactive image
ChemSpider	4528
ECHA InfoCard	100.039.767
KEGG	C19123
PubChem CID	4690
UNII	E35M7EMD3V
CompTox Dashboard (EPA)	DTXSID1040293
InChI InChI=1S/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3Key: LRUUNMYPIBZBQH-UHFFFAOYSA-N InChI=1/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3Key: LRUUNMYPIBZBQH-UHFFFAOYAP
SMILES CN1C(=O)N(OC1=O)C2=CC(=C(C=C2)Cl)Cl
Properties
Chemical formula	C₉H₆Cl₂N₂O₃
Molar mass	261.06 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references

Chemical compound

Methazole (C₉H₆Cl₂N₂O₃) is an obsolete herbicide in the family of herbicides known as oxadiazolones. It was used as a post-emergent treatment for controlling weeds.

References

^ "Methazole". University of Hertfordshire.

Pest control: herbicides

FOP herbicides	chlorazifop cyhalofop diclofop fenoxaprop fluazifop haloxyfop quizalofop
DIM herbicides	sethoxydim

Protox inhibitors

Nitrophenyl ethers	acifluorfen bifenox fluorodifen fomesafen lactofen nitrofen oxyfluorfen
Pyrimidinediones	butafenacil saflufenacil
Triazolinones	carfentrazone sulfentrazone

Pyridines

Quaternary

Photosystem I inhibitors	cyperquat diquat paraquat

Triazines

Photosystem II inhibitors	ametryn atrazine cyanazine hexazinone prometon prometryn propazine simazine simetryn terbuthylazine terbutryn metamitron

Ureas

Photosystem II inhibitors	chlortoluron DCMU difenoxuron isoproturon linuron monuron monolinuron tebuthiuron
ALS inhibitors	chlorsulfuron flazasulfuron metsulfuron-methyl sulfometuron methyl tribenuron

Others

This article about a heterocyclic compound is a stub. You can help Misplaced Pages by expanding it.

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