(S)-5-amino-1'-((2-(trimethylsilyl)ethoxy)methyl)-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one
≥95%
- Product Code: 82113
CAS:
939016-96-3
Molecular Weight: | 381.55 g./mol | Molecular Formula: | C₂₁H₂₇N₃O₂Si |
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Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. Its structure is particularly valuable in the development of small molecule inhibitors targeting specific enzymes or receptors involved in disease pathways. Researchers often employ it in the design and optimization of drug candidates, especially for conditions like cancer, inflammation, and neurological disorders. The trimethylsilyl ethoxymethyl (SEM) protecting group in its structure enhances its stability during synthetic processes, making it a versatile building block in organic synthesis. Additionally, its spirocyclic indene-pyrrolopyridinone core contributes to its potential in creating molecules with improved pharmacokinetic properties and target selectivity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $824.22 |
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(S)-5-amino-1'-((2-(trimethylsilyl)ethoxy)methyl)-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. Its structure is particularly valuable in the development of small molecule inhibitors targeting specific enzymes or receptors involved in disease pathways. Researchers often employ it in the design and optimization of drug candidates, especially for conditions like cancer, inflammation, and neurological disorders. The trimethylsilyl ethoxymethyl (SEM) protecting group in its structure enhances its stability during synthetic processes, making it a versatile building block in organic synthesis. Additionally, its spirocyclic indene-pyrrolopyridinone core contributes to its potential in creating molecules with improved pharmacokinetic properties and target selectivity.
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