(R)-2-Oxiranylanisole

97%

Reagent Code: #229876
label
Alias (R)-α-(2-epoxyethyl)anisole; (R)-glycidylphenyl ether
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CAS Number 71031-02-2

science Other reagents with same CAS 71031-02-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.17 g/mol
Formula C₉H₁₀O₂
badge Registry Numbers
MDL Number MFCD06659025
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its epoxide functionality allows for ring-opening reactions with nucleophiles, enabling the formation of complex chiral molecules. Commonly employed in the synthesis of beta-blockers and other bioactive compounds where stereochemistry is critical. Also utilized in the preparation of chiral ligands and catalysts for asymmetric synthesis. Its methoxy-substituted aromatic ring enhances reactivity and selectivity in certain coupling reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿2,200.00
25g
10-20 days ฿9,590.00
100g
10-20 days ฿30,550.00
(R)-2-Oxiranylanisole
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Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its epoxide functionality allows for ring-opening reactions with nucleophiles, enabling the formation of complex chiral molecules. Commonly employed in the synthesis of beta-blockers and other bioactive compounds where stereochemistry is critical. Also utilized in the preparation of chiral ligands and catalysts for asymmetric synthesis. Its methoxy-substituted aromatic ring enhances

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its epoxide functionality allows for ring-opening reactions with nucleophiles, enabling the formation of complex chiral molecules. Commonly employed in the synthesis of beta-blockers and other bioactive compounds where stereochemistry is critical. Also utilized in the preparation of chiral ligands and catalysts for asymmetric synthesis. Its methoxy-substituted aromatic ring enhances reactivity and selectivity in certain coupling reactions.

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