1-(Isothiocyanatomethyl)-3-(trifluoromethyl)benzene

95%

Reagent Code: #200874
fingerprint
CAS Number 2740-85-4

science Other reagents with same CAS 2740-85-4

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to the reactivity of the isothiocyanate group. Its trifluoromethyl moiety enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Also employed in the preparation of covalent inhibitors where the isothiocyanate group reacts selectively with nucleophilic amino acid residues in target proteins. Additionally, it serves as a building block in organic synthesis for constructing heterocyclic compounds with potential biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿28,000.00
1-(Isothiocyanatomethyl)-3-(trifluoromethyl)benzene
No image available

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to the reactivity of the isothiocyanate group. Its trifluoromethyl moiety enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Also employed in the preparation of covalent inhibitors where the isothiocyanate group reacts selectively with nucleophilic amino acid residues in target proteins. Additionally,

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides due to the reactivity of the isothiocyanate group. Its trifluoromethyl moiety enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Also employed in the preparation of covalent inhibitors where the isothiocyanate group reacts selectively with nucleophilic amino acid residues in target proteins. Additionally, it serves as a building block in organic synthesis for constructing heterocyclic compounds with potential biological activity.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...