2-(Benzhydrylsulfinyl)acetic acid

97%

Reagent Code: #116051
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CAS Number 63547-24-0

science Other reagents with same CAS 63547-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.34 g/mol
Formula C₁₅H₁₄O₃S
badge Registry Numbers
MDL Number MFCD09037258
thermostat Physical Properties
Boiling Point 539.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description 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.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,250.00
inventory 1g
10-20 days ฿500.00
inventory 50g
10-20 days ฿8,400.00
inventory 250mg
10-20 days ฿300.00
inventory 10g
10-20 days ฿2,100.00

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2-(Benzhydrylsulfinyl)acetic acid
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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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