Phenyl(4-bromophenyl)carbamate

95%

  • Product Code: 84683
  CAS:    50882-29-6
Molecular Weight: 292.13 g./mol Molecular Formula: C₁₃H₁₀BrNO₂
EC Number: MDL Number: MFCD00017806
Melting Point: 154 °C Boiling Point: 359.6±34.0 °C(Predicted)
Density: 1.532±0.06 g/cm3(Predicted) Storage Condition: 2-8°C
Product Description: Phenyl(4-bromophenyl)carbamate is primarily utilized in the field of organic synthesis as an intermediate for the preparation of more complex chemical compounds. It is often employed in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require specific carbamate functionalities. Additionally, this compound finds application in the production of agrochemicals, where it serves as a building block for creating pesticides or herbicides with enhanced efficacy. Its role in material science is also notable, as it can be used to modify polymers or coatings to achieve desired properties such as durability or chemical resistance. In research, it is a valuable reagent for studying reaction mechanisms involving carbamate groups.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿9,360.00
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0.250 10-20 days ฿16,380.00
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1.000 10-20 days ฿32,760.00
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Phenyl(4-bromophenyl)carbamate
Phenyl(4-bromophenyl)carbamate is primarily utilized in the field of organic synthesis as an intermediate for the preparation of more complex chemical compounds. It is often employed in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require specific carbamate functionalities. Additionally, this compound finds application in the production of agrochemicals, where it serves as a building block for creating pesticides or herbicides with enhanced efficacy. Its role in material science is also notable, as it can be used to modify polymers or coatings to achieve desired properties such as durability or chemical resistance. In research, it is a valuable reagent for studying reaction mechanisms involving carbamate groups.
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