3-(Tert-butyl)-4-(2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

  • Product Code: 70619
  CAS:    1246888-90-3
Molecular Weight: 330.36 g./mol Molecular Formula: C₁₉H₂₃O₃P
EC Number: MDL Number: MFCD30748198
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, avoid light, store in inert gas
Product Description: This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate or building block in the development of complex molecules. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it valuable for constructing phosphorus-containing heterocycles, which are essential in various pharmaceutical and agrochemical applications. It is often employed in catalytic processes or as a precursor for synthesizing ligands used in coordination chemistry. Additionally, its tert-butyl and dimethoxyphenyl groups enhance its stability and reactivity, making it suitable for creating specialized compounds with potential biological activities. Researchers also explore its use in designing materials with specific electronic or optical properties due to its aromatic and heterocyclic nature.
Product Specification:
Test Specification
APPEARANCE White to pale yellow solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $39.33
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0.250 10-20 days $73.54
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1.000 10-20 days $248.93
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3-(Tert-butyl)-4-(2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate or building block in the development of complex molecules. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it valuable for constructing phosphorus-containing heterocycles, which are essential in various pharmaceutical and agrochemical applications. It is often employed in catalytic processes or as a precursor for synthesizing ligands used in coordination chemistry. Additionally, its tert-butyl and dimethoxyphenyl groups enhance its stability and reactivity, making it suitable for creating specialized compounds with potential biological activities. Researchers also explore its use in designing materials with specific electronic or optical properties due to its aromatic and heterocyclic nature.
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