benzyl 4-mercapto-2-methylbutan-2-ylcarbamate

Reagent Code: #52737
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CAS Number 1226913-81-0

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Weight 253.36 g/mol
Formula C₁₃H₁₉NO₂S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring both a carbamate group and a thiol group, makes it valuable for constructing compounds with specific functional properties. In pharmaceutical research, it is often employed in the development of drug candidates, particularly those targeting enzymes or receptors where the thiol group can play a crucial role in binding interactions. Additionally, it is used in material science for modifying surfaces or polymers, where the thiol group can facilitate attachment to other materials or create cross-linked networks. Its versatility also extends to agrochemical research, where it may be incorporated into the synthesis of pesticides or herbicides to enhance their efficacy or stability.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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benzyl 4-mercapto-2-methylbutan-2-ylcarbamate
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring both a carbamate group and a thiol group, makes it valuable for constructing compounds with specific functional properties. In pharmaceutical research, it is often employed in the development of drug candidates, particularly those targeting enzymes or receptors where the thiol group can play a crucial role in binding inte

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring both a carbamate group and a thiol group, makes it valuable for constructing compounds with specific functional properties. In pharmaceutical research, it is often employed in the development of drug candidates, particularly those targeting enzymes or receptors where the thiol group can play a crucial role in binding interactions. Additionally, it is used in material science for modifying surfaces or polymers, where the thiol group can facilitate attachment to other materials or create cross-linked networks. Its versatility also extends to agrochemical research, where it may be incorporated into the synthesis of pesticides or herbicides to enhance their efficacy or stability.

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