Methyl (R)-2-amino-2-(3-hydroxyphenyl)acetate hydrochloride

95%

Reagent Code: #37555
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CAS Number 136057-18-6

science Other reagents with same CAS 136057-18-6

blur_circular Chemical Specifications

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Weight 217.65 g/mol
Formula C₉H₁₂ClNO₃
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description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a chiral center and a hydroxyl group, makes it a valuable intermediate in the production of enantiomerically pure drugs. It is often employed in the creation of compounds targeting neurological and cardiovascular diseases, where stereochemistry plays a critical role in efficacy and safety. Additionally, it serves as a building block in organic synthesis for the development of peptidomimetics and other bioactive molecules. Its hydrochloride form enhances stability and solubility, facilitating its use in various experimental and industrial processes.

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inventory 50mg
10-20 days ฿12,717.00

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Methyl (R)-2-amino-2-(3-hydroxyphenyl)acetate hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a chiral center and a hydroxyl group, makes it a valuable intermediate in the production of enantiomerically pure drugs. It is often employed in the creation of compounds targeting neurological and cardiovascular diseases, where stereochemistry plays a critical role in efficacy and safety. Additionally, it serves as a building block in organic synthes

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a chiral center and a hydroxyl group, makes it a valuable intermediate in the production of enantiomerically pure drugs. It is often employed in the creation of compounds targeting neurological and cardiovascular diseases, where stereochemistry plays a critical role in efficacy and safety. Additionally, it serves as a building block in organic synthesis for the development of peptidomimetics and other bioactive molecules. Its hydrochloride form enhances stability and solubility, facilitating its use in various experimental and industrial processes.

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