5-(Chloromethyl)-3-(4-ethylphenyl)-1,2,4-oxadiazole

95%

Reagent Code: #165980
fingerprint
CAS Number 854137-69-2

science Other reagents with same CAS 854137-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.67 g/mol
Formula C₁₁H₁₁ClN₂O
badge Registry Numbers
MDL Number MFCD07312769
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anticonvulsant and anti-inflammatory properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for constructing heterocyclic compounds. It is also employed in agrochemical research for designing novel pesticides due to its stability and reactivity. The chloromethyl group enables alkylation reactions, facilitating conjugation with other molecular fragments in drug design and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿15,550.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(Chloromethyl)-3-(4-ethylphenyl)-1,2,4-oxadiazole
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anticonvulsant and anti-inflammatory properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for constructing heterocyclic compounds. It is also employed in agrochemical research for designing novel pesticides due to its stability and reactivity. The chloromethyl group enables alkylation reactions, facilitating conjug

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anticonvulsant and anti-inflammatory properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for constructing heterocyclic compounds. It is also employed in agrochemical research for designing novel pesticides due to its stability and reactivity. The chloromethyl group enables alkylation reactions, facilitating conjugation with other molecular fragments in drug design and development.

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...