2-(2-Nitrophenyl)oxirane

≥98%

Reagent Code: #216064
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CAS Number 39830-70-1

science Other reagents with same CAS 39830-70-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.15 g/mol
Formula C₈H₇NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in complex molecule construction. It is also employed in the development of photoresponsive compounds due to the presence of the nitrophenyl group, which can undergo light-induced transformations. This property makes it useful in research related to photolabile protecting groups and smart materials. Additionally, it serves as a building block in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿8,010.00
1g
10-20 days ฿21,380.00
2-(2-Nitrophenyl)oxirane
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in complex molecule construction. It is also employed in the development of photoresponsive compounds due to the presence of the nitrophenyl group, which can undergo light-induced transformations. This property makes it useful in research related to photolabile protecting gr

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in complex molecule construction. It is also employed in the development of photoresponsive compounds due to the presence of the nitrophenyl group, which can undergo light-induced transformations. This property makes it useful in research related to photolabile protecting groups and smart materials. Additionally, it serves as a building block in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory conditions.

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