(R)-2-Amino-2-(4-bromophenyl)aceticacid

97%

Reagent Code: #232009
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CAS Number 1260220-71-0

science Other reagents with same CAS 1260220-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.06 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD07371734
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs where stereochemistry plays a critical role in biological activity. Its structure features both an amino group and a carboxylic acid on the same carbon, making it suitable for peptide-like coupling reactions. The presence of the bromophenyl group allows for further functionalization via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. Commonly employed in research settings for designing bioactive compounds, including potential antiviral or anticancer agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,880.00
inventory 1g
10-20 days ฿18,200.00
inventory 5g
10-20 days ฿48,820.00
inventory 10g
10-20 days ฿91,430.00
inventory 250mg
10-20 days ฿8,200.00
(R)-2-Amino-2-(4-bromophenyl)aceticacid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs where stereochemistry plays a critical role in biological activity. Its structure features both an amino group and a carboxylic acid on the same carbon, making it suitable for peptide-like coupling reactions. The presence of the bromophenyl group allows for further functionalization via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. Co

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs where stereochemistry plays a critical role in biological activity. Its structure features both an amino group and a carboxylic acid on the same carbon, making it suitable for peptide-like coupling reactions. The presence of the bromophenyl group allows for further functionalization via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. Commonly employed in research settings for designing bioactive compounds, including potential antiviral or anticancer agents.

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