4'-(Bromomethyl)-2-chloro-1,1'-biphenyl
90%
- Product Code: 45725
CAS:
210113-71-6
Molecular Weight: | 281.5755 g./mol | Molecular Formula: | C₁₃H₁₀BrCl |
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EC Number: | MDL Number: | MFCD15146809 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both bromomethyl and chloro substituents, makes it a versatile building block for constructing more complex molecules. In pharmaceutical research, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to undergo various chemical reactions, such as nucleophilic substitution or coupling reactions. Additionally, it is utilized in the synthesis of specialty chemicals and materials, where its biphenyl core contributes to the stability and functionality of the final product. Its applications are typically limited to controlled laboratory or industrial settings due to its reactive nature.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,156.00 |
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4'-(Bromomethyl)-2-chloro-1,1'-biphenyl
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both bromomethyl and chloro substituents, makes it a versatile building block for constructing more complex molecules. In pharmaceutical research, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to undergo various chemical reactions, such as nucleophilic substitution or coupling reactions. Additionally, it is utilized in the synthesis of specialty chemicals and materials, where its biphenyl core contributes to the stability and functionality of the final product. Its applications are typically limited to controlled laboratory or industrial settings due to its reactive nature.
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