1-Allylpyrrolidin-2-one

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Reagent Code: #137492
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CAS Number 2687-97-0

science Other reagents with same CAS 2687-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.17 g/mol
Formula C₇H₁₁NO
badge Registry Numbers
MDL Number MFCD00152226
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex nitrogen-containing molecules. It is also employed in the development of active ingredients in agrochemicals and in the synthesis of specialty polymers. Due to the reactivity of the allyl and carbonyl groups, it participates in cyclization, addition, and substitution reactions, which are key in creating heterocyclic compounds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,820.00
inventory 5g
10-20 days ฿9,890.00
inventory 25g
10-20 days ฿37,480.00

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1-Allylpyrrolidin-2-one
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex nitrogen-containing molecules. It is also employed in the development of active ingredients in agrochemicals and in the synthesis of specialty polymers. Due to the reactivity of the allyl and carbonyl groups, it participates in cyclization, addition, and substitution r

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex nitrogen-containing molecules. It is also employed in the development of active ingredients in agrochemicals and in the synthesis of specialty polymers. Due to the reactivity of the allyl and carbonyl groups, it participates in cyclization, addition, and substitution reactions, which are key in creating heterocyclic compounds with potential biological activity.

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