2-METHOXYBENZYLZINC CHLORIDE

0.5MTHF

Reagent Code: #88766
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CAS Number 312693-15-5

science Other reagents with same CAS 312693-15-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.00 g/mol
Formula C₈H₉ClOZn
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MDL Number MFCD01319884
inventory_2 Storage & Handling
Density 0.937 g/mL at 25 °C
Storage 2-8°C, inflated

description Product Description

This chemical is primarily used in organic synthesis as a reagent for introducing the 2-methoxybenzyl group into various compounds. It is particularly valuable in cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. This makes it useful in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it can be employed in the preparation of intermediates for drug development, where the 2-methoxybenzyl moiety is a key structural component. Its reactivity with a range of electrophiles allows for versatile applications in constructing diverse molecular frameworks.

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inventory 50ml
10-20 days ฿15,282.00

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2-METHOXYBENZYLZINC CHLORIDE
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This chemical is primarily used in organic synthesis as a reagent for introducing the 2-methoxybenzyl group into various compounds. It is particularly valuable in cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. This makes it useful in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it can be employed in the preparation of intermediates for drug development, where the 2-methoxybenzyl moie

This chemical is primarily used in organic synthesis as a reagent for introducing the 2-methoxybenzyl group into various compounds. It is particularly valuable in cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. This makes it useful in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, it can be employed in the preparation of intermediates for drug development, where the 2-methoxybenzyl moiety is a key structural component. Its reactivity with a range of electrophiles allows for versatile applications in constructing diverse molecular frameworks.

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