(S)-2-Benzyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole

97%

Reagent Code: #38344
fingerprint
CAS Number 1239015-83-8

science Other reagents with same CAS 1239015-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.3608 g/mol
Formula C₁₆H₁₄N₂S
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research due to its potential biological activity. It is often explored for its role as a chiral building block in the synthesis of more complex molecules, particularly those targeting neurological and cardiovascular diseases. Its structural framework is valuable in designing inhibitors for specific enzymes or receptors, making it a key intermediate in drug discovery. Additionally, it is studied for its potential antimicrobial and anti-inflammatory properties, contributing to the development of novel therapeutic agents. Researchers also investigate its use in asymmetric synthesis, leveraging its chiral center to produce enantiomerically pure compounds for advanced medicinal chemistry applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,059.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-2-Benzyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole
No image available
This compound is primarily utilized in pharmaceutical research due to its potential biological activity. It is often explored for its role as a chiral building block in the synthesis of more complex molecules, particularly those targeting neurological and cardiovascular diseases. Its structural framework is valuable in designing inhibitors for specific enzymes or receptors, making it a key intermediate in drug discovery. Additionally, it is studied for its potential antimicrobial and anti-inflammatory properties, contributing to the development of novel therapeutic agents. Researchers also investigate its use in asymmetric synthesis, leveraging its chiral center to produce enantiomerically pure compounds for advanced medicinal chemistry 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...