3-METHOXYBENZYLZINC CHLORIDE

0.5MTHF

Reagent Code: #88771
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CAS Number 312693-16-6

science Other reagents with same CAS 312693-16-6

blur_circular Chemical Specifications

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Weight 222.00 g/mol
Formula C₈H₉ClOZn
badge Registry Numbers
MDL Number MFCD01319883
inventory_2 Storage & Handling
Density 0.96 g/mL at 25 °C
Storage 2-8°C, inflated

description Product Description

3-Methoxybenzylzinc chloride is primarily used in organic synthesis as a versatile reagent for introducing the 3-methoxybenzyl group into various molecules. It is commonly employed in cross-coupling reactions, such as Negishi coupling, to form carbon-carbon bonds efficiently. This compound is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals, where the 3-methoxybenzyl moiety is a key structural component. Its stability and reactivity make it a valuable tool for constructing aromatic systems with specific substitution patterns, enabling the development of compounds with desired biological or physical properties.

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inventory 50ml
10-20 days ฿15,246.00

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3-METHOXYBENZYLZINC CHLORIDE
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3-Methoxybenzylzinc chloride is primarily used in organic synthesis as a versatile reagent for introducing the 3-methoxybenzyl group into various molecules. It is commonly employed in cross-coupling reactions, such as Negishi coupling, to form carbon-carbon bonds efficiently. This compound is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals, where the 3-methoxybenzyl moiety is a key structural component. Its stability and reac

3-Methoxybenzylzinc chloride is primarily used in organic synthesis as a versatile reagent for introducing the 3-methoxybenzyl group into various molecules. It is commonly employed in cross-coupling reactions, such as Negishi coupling, to form carbon-carbon bonds efficiently. This compound is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and fine chemicals, where the 3-methoxybenzyl moiety is a key structural component. Its stability and reactivity make it a valuable tool for constructing aromatic systems with specific substitution patterns, enabling the development of compounds with desired biological or physical properties.

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