3-[[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester

95%

Reagent Code: #78656
fingerprint
CAS Number 1263101-57-0

science Other reagents with same CAS 1263101-57-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 619.7 g/mol
Formula C₂₆H₄₂INO₄SSi
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its complex structure, which makes it suitable for developing novel therapeutic agents. Its functional groups, including the tert-butyl-dimethyl-silanyloxy and iodo-thiophene moieties, enable it to act as an intermediate in the synthesis of biologically active molecules. It is particularly valuable in the development of targeted drugs, where its unique structure can be modified to enhance binding affinity and selectivity. Additionally, its ester group allows for further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers often employ it in the study of enzyme inhibitors and receptor modulators, leveraging its potential to interact with specific biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿41,184.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-[[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester
No image available
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its complex structure, which makes it suitable for developing novel therapeutic agents. Its functional groups, including the tert-butyl-dimethyl-silanyloxy and iodo-thiophene moieties, enable it to act as an intermediate in the synthesis of biologically active molecules. It is particularly valuable in the development of targeted drugs, where its unique structure can be modified to enhance binding affinity and selectivity. Additionally, its ester group allows for further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers often employ it in the study of enzyme inhibitors and receptor modulators, leveraging its potential to interact with specific biological targets.
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...