7-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinoline
95%
- Product Code: 87698
CAS:
258515-54-7
Molecular Weight: | 226.11 g./mol | Molecular Formula: | C₁₀H₁₂BrN |
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EC Number: | MDL Number: | MFCD15474923 | |
Melting Point: | Boiling Point: | 265.7±40.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active molecules. Its structure, featuring a bromine atom and a tetrahydroisoquinoline core, makes it a valuable building block for constructing complex organic compounds, particularly those with potential therapeutic applications. Researchers often employ it in the development of new drugs, especially in the synthesis of compounds targeting neurological disorders. Additionally, it is used in the study of chemical reactions involving halogenated heterocycles, aiding in the exploration of novel reaction pathways and mechanisms. Its versatility in synthesis makes it a useful tool in medicinal chemistry and drug discovery research.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿1,485.00 |
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0.100 | 10-20 days | ฿2,376.00 |
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0.250 | 10-20 days | ฿3,798.00 |
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7-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinoline
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active molecules. Its structure, featuring a bromine atom and a tetrahydroisoquinoline core, makes it a valuable building block for constructing complex organic compounds, particularly those with potential therapeutic applications. Researchers often employ it in the development of new drugs, especially in the synthesis of compounds targeting neurological disorders. Additionally, it is used in the study of chemical reactions involving halogenated heterocycles, aiding in the exploration of novel reaction pathways and mechanisms. Its versatility in synthesis makes it a useful tool in medicinal chemistry and drug discovery research.
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