2-(4-methylphenyl)-2-oxoethyl thiocyanate

≥97%

Reagent Code: #213300
fingerprint
CAS Number 6097-27-4

science Other reagents with same CAS 6097-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.25 g/mol
Formula C₁₀H₉NOS
badge Registry Numbers
MDL Number MFCD00278207
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals due to its reactive thiocyanate group and conjugated ketone functionality. Its structure allows for versatile transformations, including cyclization reactions to form heterocyclic compounds. It is also employed in the development of specialty chemicals where selective reactivity is required. Due to its lachrymatory properties, it has been explored in the formulation of irritant agents for research and defensive applications, though such uses are limited and highly regulated.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,100.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(4-methylphenyl)-2-oxoethyl thiocyanate
No image available

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals due to its reactive thiocyanate group and conjugated ketone functionality. Its structure allows for versatile transformations, including cyclization reactions to form heterocyclic compounds. It is also employed in the development of specialty chemicals where selective reactivity is required. Due to its lachrymatory properties, it has been explored in the formulation of irri

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals due to its reactive thiocyanate group and conjugated ketone functionality. Its structure allows for versatile transformations, including cyclization reactions to form heterocyclic compounds. It is also employed in the development of specialty chemicals where selective reactivity is required. Due to its lachrymatory properties, it has been explored in the formulation of irritant agents for research and defensive applications, though such uses are limited and highly regulated.

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...