3-(1,2,2-Trichlorovinyl)aniline hydrochloride

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Reagent Code: #63860
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CAS Number 81972-27-2

science Other reagents with same CAS 81972-27-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.952 g/mol
Formula C₈H₆Cl₄N
badge Registry Numbers
MDL Number MFCD09743804
thermostat Physical Properties
Boiling Point 319.9ºC
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. It is particularly valuable in the development of herbicides and insecticides, where its structure contributes to the efficacy of the final product. Additionally, it finds application in research settings for studying chemical reactions involving trichlorovinyl groups and aniline derivatives. Its hydrochloride form enhances stability and solubility, making it suitable for use in controlled laboratory environments.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,490.00
inventory 200mg
10-20 days ฿540.00
inventory 1g
10-20 days ฿1,692.00

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3-(1,2,2-Trichlorovinyl)aniline hydrochloride
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. It is particularly valuable in the development of herbicides and insecticides, where its structure contributes to the efficacy of the final product. Additionally, it finds application in research settings for studying chemical reactions involving trichlorovinyl groups and aniline derivatives. Its hydrochloride form enhances stability and solubility, making it sui

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. It is particularly valuable in the development of herbicides and insecticides, where its structure contributes to the efficacy of the final product. Additionally, it finds application in research settings for studying chemical reactions involving trichlorovinyl groups and aniline derivatives. Its hydrochloride form enhances stability and solubility, making it suitable for use in controlled laboratory environments.

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