(R)-1-(2,6-Dimethylphenoxy)propan-2-amine hydrochloride

95%

Reagent Code: #230892
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CAS Number 81771-86-0

science Other reagents with same CAS 81771-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.72 g/mol
Formula C₁₁H₁₈ClNO
badge Registry Numbers
MDL Number MFCD18379555
thermostat Physical Properties
Melting Point 202-204 °C
inventory_2 Storage & Handling
Storage Room temperature, inert atmosphere

description Product Description

Used primarily as an intermediate in the synthesis of certain pharmaceuticals, particularly beta-blockers, which are medications designed to treat cardiovascular conditions such as hypertension, arrhythmias, and angina. Its chiral structure makes it valuable in producing enantiomerically pure drugs, improving efficacy and reducing side effects. It also finds use in research settings for developing new chiral amines and studying stereoselective reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿15,390.00
1g
10-20 days ฿57,740.00
250mg
10-20 days ฿23,090.00
(R)-1-(2,6-Dimethylphenoxy)propan-2-amine hydrochloride
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Used primarily as an intermediate in the synthesis of certain pharmaceuticals, particularly beta-blockers, which are medications designed to treat cardiovascular conditions such as hypertension, arrhythmias, and angina. Its chiral structure makes it valuable in producing enantiomerically pure drugs, improving efficacy and reducing side effects. It also finds use in research settings for developing new chiral amines and studying stereoselective reactions.

Used primarily as an intermediate in the synthesis of certain pharmaceuticals, particularly beta-blockers, which are medications designed to treat cardiovascular conditions such as hypertension, arrhythmias, and angina. Its chiral structure makes it valuable in producing enantiomerically pure drugs, improving efficacy and reducing side effects. It also finds use in research settings for developing new chiral amines and studying stereoselective reactions.

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