| Identification | More | [Name]
Cymiazole | [CAS]
61676-87-7 | [Synonyms]
2,4-dimethyl-n-(3-methyl-2(3h)-thiazolylidene)benzenamine
3-METHYL-2-(2,4-DIMETHYLPHENYLIMINO) THIAZOLINE
CYMIAZOL
CYMIAZOLE
n-(3-methyl-3h-thiazol-2-ylidene)-2,5-xylidine
2,4-dimethyl-n-(3-methyl-2(3h)-thiazolylidene)-benzenamin
besuntol
cga50439
cymiazolhydrochloride
n-2,3-dihydro-3-methyl-1,3-thiazol-2-ylidene-2,4-xylidene
n-3-methyl-4-thiazol-2-ylidene-2,4-xylidene
tifatol
xymiazol
2-(2,4-dimethylphenyl-imino)-3-methyl-thiazoline
TIFATOL OR CYMIAZOL
CYMYAZOLE
2,4-Dimethyl-N-(3-methyl-4-thiazolin-2-ylidene)benzenamine
2,4-Dimethyl-N-(3-methylthiazol-2(3H)-ylidene)benzenamine
Xymiazole | [EINECS(EC#)]
262-890-9 | [Molecular Formula]
C12H14N2S | [MDL Number]
MFCD01311800 | [Molecular Weight]
218.32 | [MOL File]
61676-87-7.mol |
| Chemical Properties | Back Directory | [Melting point ]
44 °C | [Boiling point ]
354.0±52.0 °C(Predicted) | [density ]
1.11±0.1 g/cm3(Predicted) | [form ]
neat | [pka]
1.92±0.20(Predicted) | [BRN ]
1213211 | [Henry's Law Constant]
1.5×102 mol/(m3Pa) at 25℃, Ebert et al. (2023) | [Major Application]
agriculture
environmental | [InChI]
1S/C12H14N2S/c1-9-4-5-11(10(2)8-9)13-12-14(3)6-7-15-12/h4-8H,1-3H3/b13-12- | [InChIKey]
YUAUPYJCVKNAEC-SEYXRHQNSA-N | [SMILES]
CN1C=CSC1=Nc2ccc(C)cc2C | [CAS DataBase Reference]
61676-87-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
22 | [WGK Germany ]
3 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral |
| Hazard Information | Back Directory | [Description]
Cymiazol is an acaricide. It is moderately soluble in water and volatile. It does not tend to be persistent in soil systems but may be in some water systems. It is not susceptible to hydrolysis. It is moderately toxic to mammals and may bioaccumulate. It is an eye and skin irritant. It shows a moderate level of toxicity to birds, fish and honeybees. | [Uses]
Acaricide. | [Production Methods]
The production of cymiazol involves the synthesis of its core structure: an iminophenyl thiazolidine derivative. The process typically starts with the preparation of a 2,4-dimethylphenyl precursor, which is then reacted with a thiazole ring system through a condensation reaction to form the imine linkage. The final compound, N-(2,4-dimethylphenyl)-3-methyl-1,3-thiazol-2(3H)-imine, is purified and often converted into its hydrochloride salt to enhance solubility and stability for veterinary formulations. | [Mechanism of action]
Contact action. Acts on nervous system. Octopamine receptor agonist. | [Pesticide Type]
Acaricide; Insecticide; Veterinary substance |
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