(S)-1-(4-Tert-butylphenyl)ethanamine

≥98%

Reagent Code: #71089
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CAS Number 511256-37-4

science Other reagents with same CAS 511256-37-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.29 g/mol
Formula C₁₂H₁₉N
badge Registry Numbers
MDL Number MFCD06762044
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs. It plays a key role in creating compounds with specific biological activities, such as receptor agonists or antagonists. Additionally, it is employed in asymmetric catalysis to produce optically active intermediates for agrochemicals and fine chemicals. Its tert-butyl group enhances steric hindrance, making it valuable in designing molecules with improved selectivity and stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,415.00
250mg
10-20 days ฿14,688.00
1g
10-20 days ฿37,908.00
(S)-1-(4-Tert-butylphenyl)ethanamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs. It plays a key role in creating compounds with specific biological activities, such as receptor agonists or antagonists. Additionally, it is employed in asymmetric catalysis to produce optically active intermediates for agrochemicals and fine chemicals. Its tert-butyl group enhances steric hindrance, making it valuable in designing molecules with improved selectivity and st

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs. It plays a key role in creating compounds with specific biological activities, such as receptor agonists or antagonists. Additionally, it is employed in asymmetric catalysis to produce optically active intermediates for agrochemicals and fine chemicals. Its tert-butyl group enhances steric hindrance, making it valuable in designing molecules with improved selectivity and stability.

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