tert-Butyl (4-(4-chlorophenyl)-4-oxobutyl)carbamate

95%

Reagent Code: #87881
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CAS Number 1354651-37-8

science Other reagents with same CAS 1354651-37-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.78 g/mol
Formula C₁₅H₂₀ClNO₃
badge Registry Numbers
MDL Number MFCD28991786
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as an intermediate in the production of drugs that target neurological disorders, such as epilepsy and anxiety, due to its structural compatibility with molecules that interact with the central nervous system. Additionally, it is used in research settings for the preparation of novel organic compounds, aiding in the exploration of new therapeutic agents. Its role in organic synthesis often involves protection of amine groups during multi-step reactions, ensuring selective transformations in complex molecular frameworks.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,563.00
tert-Butyl (4-(4-chlorophenyl)-4-oxobutyl)carbamate
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This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as an intermediate in the production of drugs that target neurological disorders, such as epilepsy and anxiety, due to its structural compatibility with molecules that interact with the central nervous system. Additionally, it is used in research settings for the preparation of novel organic compounds, aiding in the exploration of new the

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as an intermediate in the production of drugs that target neurological disorders, such as epilepsy and anxiety, due to its structural compatibility with molecules that interact with the central nervous system. Additionally, it is used in research settings for the preparation of novel organic compounds, aiding in the exploration of new therapeutic agents. Its role in organic synthesis often involves protection of amine groups during multi-step reactions, ensuring selective transformations in complex molecular frameworks.

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