(1R)-5-bromo-1-methyl-2-trityl-isoindoline
≥99%
- Product Code: 36192
CAS:
194805-14-6
Molecular Weight: | 454.4 g./mol | Molecular Formula: | C₂₈H₂₄BrN |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 507.6℃at 760 mmHg | |
Density: | Storage Condition: | 2-8℃ |
Product Description:
(1R)-5-bromo-1-methyl-2-trityl-isoindoline is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of chiral compounds. Its structure, featuring a trityl group and a bromo substituent, makes it valuable for constructing pharmacologically active molecules, such as inhibitors or receptor modulators. The compound is often employed in asymmetric synthesis to introduce stereochemistry into target molecules, which is crucial for creating drugs with specific biological activities. Additionally, it is utilized in the preparation of isoindoline-based scaffolds, which are common in medicinal chemistry for designing compounds with potential therapeutic applications.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White to light purple powder |
PURITY | 98.5-100 |
WATER | 0 0.5 % |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿12,790.00 |
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5.000 | 10-20 days | ฿29,840.00 |
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(1R)-5-bromo-1-methyl-2-trityl-isoindoline
(1R)-5-bromo-1-methyl-2-trityl-isoindoline is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of chiral compounds. Its structure, featuring a trityl group and a bromo substituent, makes it valuable for constructing pharmacologically active molecules, such as inhibitors or receptor modulators. The compound is often employed in asymmetric synthesis to introduce stereochemistry into target molecules, which is crucial for creating drugs with specific biological activities. Additionally, it is utilized in the preparation of isoindoline-based scaffolds, which are common in medicinal chemistry for designing compounds with potential therapeutic applications.
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