(R)-Styrene oxide

98%

Reagent Code: #229797
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CAS Number 20780-53-4

science Other reagents with same CAS 20780-53-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 120.15 g/mol
Formula C₈H₈O
badge Registry Numbers
MDL Number MFCD00066210
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the production of enantiomerically pure compounds. It serves as an intermediate in the synthesis of active pharmaceutical ingredients, including beta-blockers and other cardiovascular drugs. Also employed in the preparation of fine chemicals and agrochemicals where stereochemistry plays a critical role in biological activity. Its reactivity allows ring-opening reactions with nucleophiles, enabling the introduction of functional groups in a stereoselective manner. Additionally, it is used in research for asymmetric synthesis and catalysis studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿920.00
5g
10-20 days ฿3,190.00
25g
10-20 days ฿11,320.00
(R)-Styrene oxide
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Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the production of enantiomerically pure compounds. It serves as an intermediate in the synthesis of active pharmaceutical ingredients, including beta-blockers and other cardiovascular drugs. Also employed in the preparation of fine chemicals and agrochemicals where stereochemistry plays a critical role in biological activity. Its reactivity allows ring-opening reactions with nucleophiles, enabling the in

Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the production of enantiomerically pure compounds. It serves as an intermediate in the synthesis of active pharmaceutical ingredients, including beta-blockers and other cardiovascular drugs. Also employed in the preparation of fine chemicals and agrochemicals where stereochemistry plays a critical role in biological activity. Its reactivity allows ring-opening reactions with nucleophiles, enabling the introduction of functional groups in a stereoselective manner. Additionally, it is used in research for asymmetric synthesis and catalysis studies.

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