(R)-tert-Butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate

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Reagent Code: #37288
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CAS Number 1306763-30-3

science Other reagents with same CAS 1306763-30-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.32 g/mol
Formula C₁₅H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD28502614
thermostat Physical Properties
Boiling Point 357.7±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a cyano group and a carbamate moiety, makes it valuable for constructing complex organic frameworks with high stereochemical control. It is often employed in the preparation of enantiomerically pure compounds, which are crucial in the production of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, its stability and reactivity under various conditions make it suitable for use in multi-step synthetic processes, contributing to the efficient and scalable production of therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,277.00
inventory 250mg
10-20 days ฿4,563.00

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(R)-tert-Butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a cyano group and a carbamate moiety, makes it valuable for constructing complex organic frameworks with high stereochemical control. It is often employed in the preparation of enantiomerically pure compounds, which are crucial in the production of drugs targeting specific biologica

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a cyano group and a carbamate moiety, makes it valuable for constructing complex organic frameworks with high stereochemical control. It is often employed in the preparation of enantiomerically pure compounds, which are crucial in the production of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, its stability and reactivity under various conditions make it suitable for use in multi-step synthetic processes, contributing to the efficient and scalable production of therapeutic agents.

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