(1-(3-bromophenyl)cyclobutyl)methanamine hydrochloride
95%
- Product Code: 148912
CAS:
915402-09-4
| Molecular Weight: | 276.6 g./mol | Molecular Formula: | C₁₁H₁₅BrClN |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used primarily as a research chemical in organic synthesis and medicinal chemistry, this compound serves as a key intermediate in the development of pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable for constructing complex molecules with potential activity as neuroactive agents. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or secondary amines for structure-activity relationship studies. Due to the presence of the bromophenyl group, it is also employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic diversity. Its cyclobutyl backbone introduces conformational rigidity, which can enhance selectivity and metabolic stability in drug candidates. Mainly utilized in laboratory settings, it is not intended for therapeutic use.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White solid |
| Purity (%) | 95-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $513.53 |
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| 0.250 | 10-20 days | $325.56 |
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(1-(3-bromophenyl)cyclobutyl)methanamine hydrochloride
Used primarily as a research chemical in organic synthesis and medicinal chemistry, this compound serves as a key intermediate in the development of pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable for constructing complex molecules with potential activity as neuroactive agents. The amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, or secondary amines for structure-activity relationship studies. Due to the presence of the bromophenyl group, it is also employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic diversity. Its cyclobutyl backbone introduces conformational rigidity, which can enhance selectivity and metabolic stability in drug candidates. Mainly utilized in laboratory settings, it is not intended for therapeutic use.
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| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
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