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Home > Encyclopedia > 3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride

3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride

3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride structure

3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride 

structure
  • CAS No:

    52314-67-7

  • Formula:

    C8H9Cl3O

  • Chemical Name:

    3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride

  • Synonyms:

    Cyclopropanecarbonyl chloride,3-(2,2-dichloroethenyl)-2,2-dimethyl-;3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride;3-(2,2-Dichlorovinyl)-2,2-dimethyl-1-cyclopropanecarbonyl chloride;3-(2,2-Dichlorovinyl)-2,2-dimethylcyclopropanecarbonyl chloride;2,2-Dimethyl-3-(2,2-dichlorovinyl)cyclopropanecarbonyl chloride;2,2-Dimethyl-3-(2,2-dichloroethenyl)cyclopropanecarbonyl chloride;78491-05-1

  • Categories:

    Agrochemicals  >  Pesticide Intermediates

3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride Basic Attributes

227.52

227.52

257-840-8

DTXSID1028027

Characteristics

17.07000

3.27

1.4±0.1 g/cm3

70-80°C (15 torr)

98.9±25.1 °C

1.581

Safety Information

P260, P261, P264, P270, P271, P272, P273, P280, P301+P310, P302+P352, P304+P312, P304+P340, P312, P314, P321, P330, P332+P313, P333+P313, P362, P363, P391, P403+P233, P405, P501

H301

|Danger|H301 (50%): Toxic if swallowed [Danger Acute toxicity, oral]|P260, P261, P264, P270, P271, P272, P273, P280, P301+P310, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P314, P321, P330, P332+P313, P333+P313, P362, P363, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 8 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride Use and Manufacturing

Methods of Manufacturing

Its preparation method is to prepare dipermethrin acid chloride with thionyl chloride, phosphorus trichloride or phosgene. Add permethrin acid and toluene to the reaction kettle, add catalyst, and start to pass phosgene when the temperature is raised to 80℃ under stirring. The phosgene flow rate is 4m3/h, and the temperature is maintained at 80~90℃. The reaction time is about 1.5h. At the end, stop phosgene. After cooling, the excess phosgene is blown out with nitrogen, and the reaction tail gas is recovered by the tail gas absorption device, and treated with hydrochloric acid and alkali. After stopping nitrogen flow, vacuum distillation is performed, and toluene is recovered to obtain dichlorochrysanthemumyl chloride.

Uses

Used as pesticide intermediate

Cyclopropanecarbonyl chloride, 3-(2,2-dichloroethenyl)-2,2-dimethyl-: ACTIVE

Computed Properties

Molecular Weight:227.5
XLogP3:4.3
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:225.971898
Monoisotopic Mass:225.971898
Topological Polar Surface Area:17.1
Heavy Atom Count:12
Complexity:241
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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