methyl 3-phenyloxirane-2-carboxylate

99%

Reagent Code: #205331
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CAS Number 37161-74-3

science Other reagents with same CAS 37161-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.18 g/mol
Formula C₁₀H₁₀O₃
badge Registry Numbers
EC Number 253-370-2
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals. Its epoxide ring allows for regioselective ring-opening reactions, enabling the construction of complex molecules with defined stereochemistry. Commonly employed in the synthesis of β-blockers and other bioactive compounds where stereochemical control is critical. Also utilized in the preparation of optically active α-hydroxy esters through catalytic asymmetric hydrolysis or reduction. Its phenyl and ester functionalities provide handles for further chemical modifications, making it valuable in medicinal chemistry and drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿1,040.00
1g
10-20 days ฿3,310.00
10g
10-20 days ฿16,740.00
methyl 3-phenyloxirane-2-carboxylate
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Used as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals. Its epoxide ring allows for regioselective ring-opening reactions, enabling the construction of complex molecules with defined stereochemistry. Commonly employed in the synthesis of β-blockers and other bioactive compounds where stereochemical control is critical. Also utilized in the preparation of optically active α-hydroxy esters through catalytic asymmetric hydrolysis or reduction. Its phenyl and

Used as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals. Its epoxide ring allows for regioselective ring-opening reactions, enabling the construction of complex molecules with defined stereochemistry. Commonly employed in the synthesis of β-blockers and other bioactive compounds where stereochemical control is critical. Also utilized in the preparation of optically active α-hydroxy esters through catalytic asymmetric hydrolysis or reduction. Its phenyl and ester functionalities provide handles for further chemical modifications, making it valuable in medicinal chemistry and drug discovery.

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