tert-Butyl (cis-4-hydroxycyclohexyl)(methyl)carbamate

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Reagent Code: #150574
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CAS Number 561307-54-8

science Other reagents with same CAS 561307-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.32 g/mol
Formula C₁₂H₂₃NO₃
badge Registry Numbers
MDL Number MFCD23106042
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. This compound, tert-butyl (cis-4-hydroxycyclohexyl)(methyl)carbamate, features a cis configuration with a 4-hydroxycyclohexyl ring attached to an N-methylcarbamate group protected by tert-butyl. The protecting group enables selective reactions by shielding the nitrogen, with deprotection possible in final synthesis steps. Its functional groups, including the protected amine and alcohol, facilitate further modifications for bioactive molecules. Commonly employed in medicinal chemistry as a building block for peptidomimetics, receptor modulators, protease inhibitors, and other therapeutic agents requiring stereochemical control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,080.00
inventory 250mg
10-20 days ฿10,090.00
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tert-Butyl (cis-4-hydroxycyclohexyl)(methyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. This compound, tert-butyl (cis-4-hydroxycyclohexyl)(methyl)carbamate, features a cis configuration with a 4-hydroxycyclohexyl ring attached to an N-methylcarbamate group protected by tert-butyl. The protecting group enables selective reactions by shielding the nitrogen, with deprotection possible in final synthesis steps. I

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. This compound, tert-butyl (cis-4-hydroxycyclohexyl)(methyl)carbamate, features a cis configuration with a 4-hydroxycyclohexyl ring attached to an N-methylcarbamate group protected by tert-butyl. The protecting group enables selective reactions by shielding the nitrogen, with deprotection possible in final synthesis steps. Its functional groups, including the protected amine and alcohol, facilitate further modifications for bioactive molecules. Commonly employed in medicinal chemistry as a building block for peptidomimetics, receptor modulators, protease inhibitors, and other therapeutic agents requiring stereochemical control.

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