CAS No. 78587-05-0  | Hexythiazox
CAS No. 78587-05-0  | Hexythiazox
CAS No. 78587-05-0  | Hexythiazox
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  • CAS No. 78587-05-0  | Hexythiazox
  • CAS No. 78587-05-0  | Hexythiazox
  • CAS No. 78587-05-0  | Hexythiazox

CAS No. 78587-05-0 | Hexythiazox

Name: Hexythiazox CAS No.78587-05-0 MF:C17H21ClN2O2S MW:352.88 Purity:99% Package: 5g,25g,200g,500g,1kg Worldwide Delivery

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Other Material Chemicals

Product introduction

Introduction and application of CAS No. 78587-05-0  | Hexythiazox

 

Synonyms:5-(4-chlorophenyl)-n-cyclohexyl-4-methyl-2-oxo-3-thiazolidinecarboxamidtra;

trans-5-(4-chlorophenyl)-n-cyclohexyl-4-methyl-2-oxo-3-thiazolidinecarboxami;

 

Specification:

ITEMS

SPECIFICATION

CAS

78587-05-0

MF

C17H21ClN2O2S

MW

352.88

Melting point

108-108.5°C

Boiling point

128°C

Density

1.1354

Acidity coefficient

12.77±0.20

Color

White to almost white

Solubility

DMF: 5 mg/ml, DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml, DMSO: 2 mg/ml, ethanol: 0.2 mg/ml

Flash point

100 °C

Storage condition

0-6°C

use:

Thiazolidinone acaricides. This product is broad-spectrum and has good effects on young nymphs and eggs of various spider mites, but has poor effect on adult mites. After treatment with the agent, the eggs laid by female mites cannot hatch. It mainly has contact killing effect, has good permeability to plant tissues, and has no systemic effect. The effect of the drug is slow, but the residual effect can be as long as more than 1 month. Safe for crops, feeding mites and beneficial insects. For example, to control apple red spider mites, when there are an average of 3 to 4 mites per leaf during the peak period of young nymphal mites, use 5% emulsifiable concentrate or 5% wettable powder 1500 to 2000 times liquid spray. Stop using 7 days before harvest.

production method:

It is obtained by condensing trans-5-(4-chlorophenyl)-4-methyl-2-oxothiazolidinone and cyclohexyl isocyanate as raw materials. 20g of trans 5-(4-chlorophenyl)-4-methyl-2-oxothiazolidinone and 11.9g of cyclohexyl isocyanate were added to benzene, and the reaction was stirred at room temperature. After post-treatment, 30.7g of thiazolidinone was obtained ketone. Preparation of trans-5-(4-chlorophenyl)-4-methyl-2-oxothiazolidinone: Dissolve trans-2-amino-1-p-chlorophenylpropanol in an organic solvent with an equimolar amount The sulfuric acid is condensed and dehydrated to generate trans-sulfate ester, and then reacts with carbon oxysulfide under alkaline conditions to generate thiocarbamic acid derivatives. At the same time, the intramolecular sulfur atom attacks the carbon on the phenyl group to generate p-, 5- trans-thiazolidinone. Formulated as 10% emulsifiable concentrate, 10% or 50% wettable powder.

 

Package and transportation :

Package: 5g,25g,200g,500g,1kg

Transportation: by courier/ by air/ by sea

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