2,4-Dibromobutanoic acid

95%

  • Product Code: 86607
  CAS:    63164-16-9
Molecular Weight: 245.9 g./mol Molecular Formula: C₄H₆Br₂O₂
EC Number: MDL Number: MFCD01632493
Melting Point: Boiling Point: 294.1 °C at 760 mmHg (lit.)
Density: Storage Condition: 2-8°C, inert gas
Product Description: 2,4-Dibromobutanoic acid is primarily used in organic synthesis as a building block for more complex chemical compounds. It serves as an intermediate in the production of pharmaceuticals, where it can be utilized to create active pharmaceutical ingredients (APIs) with specific therapeutic properties. Additionally, it finds application in the synthesis of agrochemicals, contributing to the development of herbicides, pesticides, and other crop protection agents. Its bromine atoms make it a valuable reagent in halogenation reactions, enabling the introduction of bromine into organic molecules for further functionalization. This compound is also employed in research laboratories for studying reaction mechanisms and developing new synthetic methodologies.
Product Specification:
Test Specification
APPEARANCE liquid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $734.30
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5.000 10-20 days $2,687.09
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2,4-Dibromobutanoic acid
2,4-Dibromobutanoic acid is primarily used in organic synthesis as a building block for more complex chemical compounds. It serves as an intermediate in the production of pharmaceuticals, where it can be utilized to create active pharmaceutical ingredients (APIs) with specific therapeutic properties. Additionally, it finds application in the synthesis of agrochemicals, contributing to the development of herbicides, pesticides, and other crop protection agents. Its bromine atoms make it a valuable reagent in halogenation reactions, enabling the introduction of bromine into organic molecules for further functionalization. This compound is also employed in research laboratories for studying reaction mechanisms and developing new synthetic methodologies.
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