3-Methyl(Thiobenzamide)

98%

Reagent Code: #207698
fingerprint
CAS Number 2362-63-2

science Other reagents with same CAS 2362-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.23 g/mol
Formula C₈H₉NS
badge Registry Numbers
MDL Number MFCD01314035
thermostat Physical Properties
Melting Point 87-89°C
Boiling Point 272.1ºC
inventory_2 Storage & Handling
Density 1.143 g/cm3
Storage 2-8ºC

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a ligand in coordination chemistry, forming complexes with transition metals that are useful in catalysis. Also employed in the development of agrochemicals and bioactive molecules due to its sulfur-containing structure, which can enhance biological activity. Its thioamide group allows for hydrogen bonding and metal coordination, making it valuable in crystal engineering and material science applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿430.00
inventory 1g
10-20 days ฿950.00
inventory 5g
10-20 days ฿4,670.00
inventory 10g
10-20 days ฿8,540.00
inventory 25g
10-20 days ฿15,720.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Methyl(Thiobenzamide)
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a ligand in coordination chemistry, forming complexes with transition metals that are useful in catalysis. Also employed in the development of agrochemicals and bioactive molecules due to its sulfur-containing structure, which can enhance biological activity. Its thioamide group allows for hydrogen bonding and metal coordination, making it valuable in crystal engineeri

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a ligand in coordination chemistry, forming complexes with transition metals that are useful in catalysis. Also employed in the development of agrochemicals and bioactive molecules due to its sulfur-containing structure, which can enhance biological activity. Its thioamide group allows for hydrogen bonding and metal coordination, making it valuable in crystal engineering and material science applications.

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...