2-(Benzhydrylsulfinyl)acetic acid

97%

  • Product Code: 116051
  CAS:    63547-24-0
Molecular Weight: 274.34 g./mol Molecular Formula: C₁₅H₁₄O₃S
EC Number: MDL Number: MFCD09037258
Melting Point: Boiling Point: 539.2°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: 2-(Benzhydrylsulfinyl)acetic acid is primarily utilized in the field of organic synthesis as a versatile intermediate. Its unique structure, featuring a benzhydryl group and a sulfinyl moiety, makes it valuable for constructing complex molecules, particularly in pharmaceutical research. It is often employed in the development of potential drug candidates, where its sulfinyl group can act as a chiral auxiliary or a directing group in asymmetric synthesis. Additionally, this compound is explored in the design of novel materials and ligands for catalysis, owing to its ability to coordinate with metal ions. Its applications extend to the study of biochemical pathways, where it serves as a model compound to understand sulfoxide behavior in biological systems.
Product Specification:
Test Specification
Appearance White To Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿300.00
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1.000 10-20 days ฿500.00
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5.000 10-20 days ฿1,250.00
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10.000 10-20 days ฿2,100.00
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50.000 10-20 days ฿8,400.00
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2-(Benzhydrylsulfinyl)acetic acid
2-(Benzhydrylsulfinyl)acetic acid is primarily utilized in the field of organic synthesis as a versatile intermediate. Its unique structure, featuring a benzhydryl group and a sulfinyl moiety, makes it valuable for constructing complex molecules, particularly in pharmaceutical research. It is often employed in the development of potential drug candidates, where its sulfinyl group can act as a chiral auxiliary or a directing group in asymmetric synthesis. Additionally, this compound is explored in the design of novel materials and ligands for catalysis, owing to its ability to coordinate with metal ions. Its applications extend to the study of biochemical pathways, where it serves as a model compound to understand sulfoxide behavior in biological systems.
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