tert-Butyl (3-hydroxycyclohexyl)carbamate

95%

Reagent Code: #146119
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CAS Number 610302-03-9

science Other reagents with same CAS 610302-03-9

blur_circular Chemical Specifications

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Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its hydroxyl and carbamate functional groups allow selective protection and coupling reactions, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly employed in the synthesis of steroids, receptor agonists, and other bioactive compounds where controlled functional group manipulation is required. Also utilized in medicinal chemistry for scaffold modification and optimization of drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,190.00
inventory 5g
10-20 days ฿4,100.00
inventory 10g
10-20 days ฿6,300.00
inventory 25g
10-20 days ฿14,200.00
inventory 100g
10-20 days ฿54,640.00

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tert-Butyl (3-hydroxycyclohexyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its hydroxyl and carbamate functional groups allow selective protection and coupling reactions, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly employed in the synthesis of steroids, receptor agonists, and other bioactive compounds where controlled functional group manipulation is required. Also utilized in medicinal chemistry for scaffo

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its hydroxyl and carbamate functional groups allow selective protection and coupling reactions, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly employed in the synthesis of steroids, receptor agonists, and other bioactive compounds where controlled functional group manipulation is required. Also utilized in medicinal chemistry for scaffold modification and optimization of drug candidates.

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